A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608151



Internal ID6995081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14739211..14740752hg38UCSC Ensembl
Innerchr6:14739211..14740752hg38UCSC Ensembl
Outerchr6:14738939..14740921hg38UCSC Ensembl
chr6:14739442..14740983hg19UCSC Ensembl
Innerchr6:14739442..14740983hg19UCSC Ensembl
Outerchr6:14739170..14741152hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12197472, essv12197478, essv12197469, essv12197462, essv12197450, essv12197474, essv12197451, essv12197467, essv12197468, essv12197465, essv12197452, essv12197446, essv12197466, essv12197459, essv12197475, essv12197480, essv12197463, essv12197453, essv12197457, essv12197449, essv12197481, essv12197448, essv12197456, essv12197454, essv12197461, essv12197464, essv12197470, essv12197473, essv12197455, essv12197477, essv12197447, essv12197460, essv12197479, essv12197458, essv12197471, essv12197476
SamplesNA19909, NA19204, HG02852, HG03280, HG03372, HG03133, HG02549, NA19130, HG02505, NA19922, HG02634, HG03045, HG02571, NA20412, NA19189, HG01384, NA18516, HG02470, HG02878, NA18907, HG03024, NA19099, NA19160, NA19309, HG02010, HG01915, HG03419, HG03108, HG03066, HG03025, HG03279, HG02013, NA19711, NA19213, HG03162, HG03303
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608151
Frequency
Sample Size2504
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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