A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657527



Internal ID9923632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31244809..31245105hg38UCSC Ensembl
chr16:31256130..31256426hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5711967, essv6148363, essv5867205, essv5498546, essv6232645, essv6103814, essv6026915, essv6229762, essv6540522, essv5721627, essv5842313, essv6433895, essv6026089, essv5694318, essv5602422, essv5758602, essv5409052, essv6082112, essv6224493, essv6334258, essv5773248, essv6049052, essv5881035, essv6325825, essv5836368, essv6350607, essv5907751, essv5449947, essv5724774, essv6304017, essv5422540, essv5568952, essv5761676, essv5447716, essv5692912, essv6201682, essv5677883, essv6170014, essv5881255, essv6412146, essv5746177, essv5758498, essv5691178, essv6179948, essv5634282, essv5880755, essv5548988, essv6085777, essv6378531, essv5513287, essv5420542
SamplesNA19703, NA19397, HG01462, NA19204, NA12414, NA19704, NA12045, NA19350, NA12004, NA19377, NA18870, NA19920, NA19374, NA19396, NA19373, NA19379, NA18519, NA18489, NA19448, NA18916, NA19138, NA18498, HG01365, NA20287, NA19904, NA19384, NA19404, NA20340, NA19372, NA19385, NA19172, HG01440, NA11993, NA19657, NA19455, NA18910, NA18871, NA18499, NA19257, NA19452, NA19625, HG01107, NA19401, NA19147, NA19360, NA19376, NA19102, NA18873, NA19116, NA19463, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657527
Frequency
Sample Size1151
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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