A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666977



Internal ID9933082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17377985..17380991hg38UCSC Ensembl
Outerchr6:17377614..17381361hg38UCSC Ensembl
Innerchr6:17378216..17381222hg19UCSC Ensembl
Outerchr6:17377845..17381592hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383748
hg193748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1076e199
Supporting Variantsessv6401885, essv6117492, essv6490699, essv6463200, essv5471493, essv6274205, essv5583926, essv6448475, essv5405714, essv5574733, essv5533459, essv5750062, essv5412143, essv5909227, essv5593018, essv5746014, essv6581773, essv6208164, essv6175684, essv5719714, essv6127411, essv5627414, essv5660920
SamplesHG00096, HG00143, HG00100, HG00151, HG00138, HG00251, HG00122, HG00247, HG00243, HG00158, HG00139, HG00120, HG00106, HG00232, HG00118, HG00253, HG00137, HG00149, HG00152, HG00126, HG00124, HG00265, HG00116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666977
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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