A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609262



Internal ID6996184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63496552..63500042hg38UCSC Ensembl
Innerchr6:63496552..63500042hg38UCSC Ensembl
Outerchr6:63496462..63500165hg38UCSC Ensembl
chr6:64206457..64209947hg19UCSC Ensembl
Innerchr6:64206457..64209947hg19UCSC Ensembl
Outerchr6:64206367..64210070hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg383491
hg193491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389805, essv12389801, essv12389808, essv12389803, essv12389806, essv12389810, essv12389809, essv12389800, essv12389807, essv12389798, essv12389799, essv12389802, essv12389804
SamplesNA19704, HG03499, HG03268, NA19901, HG03048, NA19247, HG03563, NA18879, HG02721, HG01915, NA19818, HG02107, NA19093
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609262
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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