A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665412



Internal ID9931517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55526891..55527080hg38UCSC Ensembl
Outerchr19:55526852..55527137hg38UCSC Ensembl
Innerchr19:56038258..56038447hg19UCSC Ensembl
Outerchr19:56038219..56038504hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6177956, essv5926301, essv6332971, essv6026861, essv5399776, essv6053908, essv6125042, essv6115419, essv6298594, essv6540091, essv5534125, essv6314406, essv5916878, essv5771743, essv5920118, essv6116460, essv5466034, essv5702784, essv5399366, essv6424878, essv6283952, essv6456457, essv6279134, essv5861984, essv5722932, essv6536458, essv6255850, essv6204961, essv6193049, essv5850961, essv5802170, essv5703812, essv6214516, essv6043956, essv6330616, essv6539447, essv5656527, essv5824430, essv6462864, essv6323256, essv6114625
SamplesNA12842, NA12286, NA11931, NA20802, NA18545, NA20805, NA18510, NA12413, HG01488, NA18635, NA18574, NA20768, NA20541, NA18874, NA19235, NA18617, NA19445, NA20757, HG00543, NA20521, NA20536, NA19788, NA18910, NA18948, NA20770, NA19114, NA19449, NA20581, NA12829, HG00276, NA20828, NA18536, NA18953, NA19652, NA19072, NA19010, NA12046, HG01489, NA12830, NA19004, NA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665412
Frequency
Sample Size1151
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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