A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657758



Internal ID9923863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46386979..46387139hg38UCSC Ensembl
chr11:46408529..46408689hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6513419, essv5492776, essv6403389, essv5782440, essv5613252, essv6091078, essv5427100, essv6265405, essv5900706, essv6281089, essv5978207, essv5750534, essv5409331, essv6378137, essv6323191, essv6383886, essv5582875, essv6194400, essv5427219, essv6320439, essv6434611, essv6243532, essv5422895, essv6130755, essv5854337, essv5826061, essv5811488, essv6248835, essv6392441, essv6148412, essv6191711, essv6261964, essv5914204, essv5705184
SamplesNA20588, NA20761, HG01441, NA12286, NA19664, NA11933, HG00306, NA20816, HG00115, NA20769, NA07347, NA19771, HG01083, HG00334, HG01110, NA20819, HG00156, HG00232, NA19725, HG01133, HG01136, HG00551, NA20525, HG01094, HG00324, HG01383, NA06985, HG00141, NA20815, HG01137, HG00339, NA19716, NA11843, NA07056
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657758
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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