A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610157



Internal ID6997076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101034657..101039134hg38UCSC Ensembl
Innerchr6:101035157..101038634hg38UCSC Ensembl
Outerchr6:101033657..101040134hg38UCSC Ensembl
chr6:101482533..101487010hg19UCSC Ensembl
Innerchr6:101483033..101486510hg19UCSC Ensembl
Outerchr6:101481533..101488010hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg384478
hg194478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12482201, essv12482222, essv12482288, essv12482249, essv12482317, essv12482311, essv12482304, essv12482325, essv12482344, essv12482212, essv12482283, essv12482268, essv12482266, essv12482305, essv12482198, essv12482320, essv12482243, essv12482220, essv12482287, essv12482290, essv12482314, essv12482217, essv12482291, essv12482323, essv12482275, essv12482296, essv12482193, essv12482253, essv12482239, essv12482246, essv12482308, essv12482322, essv12482327, essv12482207, essv12482245, essv12482226, essv12482310, essv12482232, essv12482319, essv12482251, essv12482321, essv12482215, essv12482205, essv12482219, essv12482189, essv12482206, essv12482210, essv12482328, essv12482242, essv12482269, essv12482337, essv12482330, essv12482260, essv12482192, essv12482247, essv12482299, essv12482199, essv12482216, essv12482224, essv12482233, essv12482286, essv12482208, essv12482200, essv12482345, essv12482213, essv12482252, essv12482223, essv12482230, essv12482306, essv12482276, essv12482318, essv12482197, essv12482194, essv12482255, essv12482301, essv12482235, essv12482284, essv12482332, essv12482236, essv12482313, essv12482274, essv12482244, essv12482231, essv12482265, essv12482258, essv12482273, essv12482334, essv12482250, essv12482241, essv12482292, essv12482196, essv12482214, essv12482281, essv12482270, essv12482261, essv12482237, essv12482309, essv12482203, essv12482339, essv12482263, essv12482340, essv12482338, essv12482335, essv12482289, essv12482191, essv12482248, essv12482227, essv12482259, essv12482342, essv12482324, essv12482293, essv12482280, essv12482298, essv12482240, essv12482228, essv12482297, essv12482257, essv12482234, essv12482262, essv12482277, essv12482282, essv12482218, essv12482238, essv12482331, essv12482336, essv12482204, essv12482285, essv12482254, essv12482190, essv12482295, essv12482279, essv12482329, essv12482343, essv12482333, essv12482300, essv12482221, essv12482341, essv12482302, essv12482316, essv12482271, essv12482256, essv12482312, essv12482264, essv12482209, essv12482315, essv12482307, essv12482229, essv12482211, essv12482303, essv12482278, essv12482272, essv12482267, essv12482195, essv12482294, essv12482326, essv12482202, essv12482225
SamplesHG03366, HG01412, NA19700, NA19703, NA18924, HG02583, HG03548, NA18861, NA19914, NA19378, HG03057, HG03300, HG03449, HG02798, HG02891, HG02012, NA20321, HG02804, HG02323, HG02476, NA19355, NA19819, HG03190, HG03100, NA20332, HG03515, HG03139, HG03577, HG02888, HG02536, NA19190, HG03372, NA19314, HG03069, NA19107, HG03199, NA19379, NA19319, HG02810, NA20320, NA19307, HG03091, HG02325, HG02840, NA19198, NA20317, HG02756, HG02620, NA19916, HG03246, NA19023, NA19138, NA20291, HG02922, HG03079, NA19922, NA19404, HG03209, HG02562, HG02561, HG03189, NA18874, HG03212, NA20340, HG03045, HG02885, NA19207, NA19172, NA19471, HG02471, HG01405, NA18520, HG02946, NA19456, HG03114, HG02943, NA19908, HG03054, HG03160, HG03061, NA19403, NA19152, HG02678, HG03547, NA19184, HG03291, HG02108, NA19236, HG03457, NA19982, NA18915, HG02144, HG03428, HG02968, HG02878, HG02757, HG03294, HG01094, HG03301, NA19114, NA18879, HG03136, HG03202, HG02577, HG03078, HG03446, HG02884, NA18853, NA19099, NA18523, HG02332, NA19095, HG02586, NA18858, HG02568, HG02484, HG01896, HG02813, NA19308, HG02613, HG02330, HG02282, NA19108, HG03461, HG03437, HG02759, NA20276, HG02546, HG02308, NA19473, HG01894, HG02721, NA19144, HG03304, NA19467, NA20281, HG03419, HG03103, HG02771, NA19117, HG03432, NA19248, NA19472, HG03066, NA19351, HG03313, HG03060, HG02462, HG02013, NA19900, HG02052, HG03162, NA18511, NA18522, HG02808, HG03439, NA19214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610157
Frequency
Sample Size2504
Observed Gain0
Observed Loss157
Observed Complex0
Frequencyn/a


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