A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637674



Internal ID6677776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3702100..3704001hg38UCSC Ensembl
Innerchr16:3702102..3704000hg38UCSC Ensembl
Outerchr16:3702099..3704003hg38UCSC Ensembl
chr16:3752101..3754002hg19UCSC Ensembl
Innerchr16:3752103..3754001hg19UCSC Ensembl
Outerchr16:3752100..3754004hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363292, essv15363291, essv15363285, essv15363280, essv15363270, essv15363293, essv15363276, essv15363284, essv15363277, essv15363278, essv15363298, essv15363282, essv15363272, essv15363265, essv15363268, essv15363281, essv15363295, essv15363288, essv15363269, essv15363301, essv15363299, essv15363275, essv15363302, essv15363266, essv15363264, essv15363297, essv15363271, essv15363286, essv15363294, essv15363267, essv15363289, essv15363279, essv15363273, essv15363283, essv15363296, essv15363287, essv15363290, essv15363274, essv15363300
SamplesHG03121, HG03548, NA19399, NA20298, HG02589, NA18870, NA19314, HG03095, HG03436, HG03385, NA19448, HG02325, HG03578, NA18868, NA19207, HG02420, NA18864, HG03114, NA19908, HG02334, NA18933, NA19184, HG02511, HG02554, NA19982, HG02450, HG02470, NA18907, HG02455, NA19380, HG03557, HG02814, HG03084, HG03063, HG03258, HG03410, HG02851, NA19431, HG03196
Known GenesTRAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637674
Frequency
Sample Size2504
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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