A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607936



Internal ID6994867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3884967..3887228hg38UCSC Ensembl
Innerchr6:3884967..3887228hg38UCSC Ensembl
Outerchr6:3884853..3887317hg38UCSC Ensembl
chr6:3885201..3887462hg19UCSC Ensembl
Innerchr6:3885201..3887462hg19UCSC Ensembl
Outerchr6:3885087..3887551hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179372, essv12179320, essv12179364, essv12179384, essv12179386, essv12179319, essv12179382, essv12179366, essv12179345, essv12179379, essv12179351, essv12179307, essv12179338, essv12179308, essv12179322, essv12179362, essv12179301, essv12179363, essv12179335, essv12179331, essv12179356, essv12179324, essv12179368, essv12179334, essv12179333, essv12179392, essv12179360, essv12179348, essv12179341, essv12179291, essv12179371, essv12179329, essv12179321, essv12179303, essv12179388, essv12179311, essv12179377, essv12179378, essv12179326, essv12179387, essv12179352, essv12179385, essv12179347, essv12179292, essv12179297, essv12179304, essv12179395, essv12179313, essv12179306, essv12179323, essv12179361, essv12179376, essv12179370, essv12179290, essv12179367, essv12179353, essv12179391, essv12179374, essv12179293, essv12179342, essv12179316, essv12179315, essv12179390, essv12179328, essv12179296, essv12179327, essv12179325, essv12179286, essv12179389, essv12179350, essv12179330, essv12179294, essv12179300, essv12179373, essv12179305, essv12179344, essv12179298, essv12179355, essv12179318, essv12179287, essv12179337, essv12179346, essv12179340, essv12179358, essv12179309, essv12179295, essv12179289, essv12179393, essv12179369, essv12179359, essv12179349, essv12179336, essv12179365, essv12179310, essv12179288, essv12179332, essv12179381, essv12179299, essv12179343, essv12179312, essv12179375, essv12179314, essv12179380, essv12179339, essv12179394, essv12179317, essv12179383, essv12179354, essv12179302, essv12179357
SamplesHG03265, HG03271, HG03514, HG01986, HG01985, HG02944, HG02628, HG01885, HG03175, HG02433, NA19704, HG02318, NA18881, HG02419, HG02836, HG02798, HG03558, HG00640, HG02870, HG02804, HG03518, HG03515, HG03193, HG03577, HG02589, NA19443, NA20356, HG03069, HG03133, NA18519, HG03385, HG03452, HG03091, HG03485, HG02549, HG03246, NA18498, NA20291, NA19038, HG02561, HG02315, HG02461, NA19235, HG01284, HG02471, HG03380, NA19189, NA19456, HG02715, HG01550, NA20318, HG01312, HG02479, HG03120, HG02977, HG02439, NA19210, NA19707, NA19403, HG01879, HG02450, HG02307, HG03081, HG02497, HG02976, NA18907, NA19114, HG02429, HG02445, NA19042, NA18499, HG03571, HG03024, HG03451, HG03046, HG03567, NA20296, HG02255, NA19401, HG02807, NA18909, HG03240, NA19108, NA19256, HG03539, HG02546, HG02314, HG02982, HG03127, HG02941, NA19467, HG01108, HG02970, HG03025, NA19468, HG03279, HG03063, HG03060, NA18873, HG02013, NA19213, HG03077, HG02051, NA19121, HG03072, HG02851, HG02805, HG02808, HG03118, NA19346
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607936
Frequency
Sample Size2504
Observed Gain0
Observed Loss110
Observed Complex0
Frequencyn/a


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