A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663161



Internal ID9929266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105382250..105382431hg38UCSC Ensembl
Outerchr13:105382093..105382584hg38UCSC Ensembl
Innerchr13:106034600..106034781hg19UCSC Ensembl
Outerchr13:106034443..106034934hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5549686, essv6152571, essv5467125, essv5599551, essv5793781, essv6465893, essv5808399, essv6085676, essv5834928, essv6460337, essv6345125, essv5582252, essv6028991, essv5805384, essv5942716, essv6074767, essv6352745, essv6346899, essv6109952, essv5882164, essv5720421, essv6042313, essv5457756, essv5644701, essv5815653, essv6099381, essv5433492, essv5583575, essv5448293, essv6535341, essv5421164, essv5879974, essv6469173, essv6482960, essv5516286, essv6351826, essv6013018, essv5455450, essv5958285, essv6146789, essv6180969, essv5842744, essv6137349, essv5532350, essv6451021, essv5851792, essv5413674, essv6179387, essv5519193, essv5882848, essv5937059, essv5856959, essv5909635, essv5551793, essv5887344
SamplesHG01173, HG00608, HG00671, NA18596, NA18530, NA18606, NA18602, NA19076, HG00501, HG01351, HG00689, HG00369, HG00277, NA19720, HG00148, HG01170, HG00419, HG00464, HG00108, HG01124, HG01353, HG00543, HG01183, HG01136, NA18544, HG00282, HG00653, HG00475, HG00533, HG00583, HG01390, HG00284, HG01073, HG01101, HG00525, HG00246, HG00611, HG00476, NA19834, HG00580, HG00375, HG01375, HG00319, NA18610, HG00339, HG00125, NA19818, HG00707, HG00614, HG00513, HG00421, HG01082, NA18624, HG00345, NA18549
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663161
Frequency
Sample Size1151
Observed Gain0
Observed Loss55
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer