A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620935



Internal ID7007805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85403511..85404885hg38UCSC Ensembl
Innerchr9:85403523..85404874hg38UCSC Ensembl
Outerchr9:85403500..85404897hg38UCSC Ensembl
chr9:88018426..88019800hg19UCSC Ensembl
Innerchr9:88018438..88019789hg19UCSC Ensembl
Outerchr9:88018415..88019812hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13543285, essv13543307, essv13543295, essv13543297, essv13543313, essv13543312, essv13543294, essv13543306, essv13543292, essv13543304, essv13543293, essv13543301, essv13543298, essv13543311, essv13543309, essv13543290, essv13543305, essv13543302, essv13543300, essv13543286, essv13543303, essv13543291, essv13543310, essv13543287, essv13543296, essv13543288, essv13543289, essv13543308, essv13543299, essv13543314
SamplesHG04210, HG01610, NA21100, HG00367, HG02734, HG02688, HG03874, NA12283, HG00311, HG00148, HG02736, HG01525, HG00326, HG00188, NA20810, NA11894, HG00140, HG00141, HG01936, NA21113, NA20851, HG03866, HG00353, HG00107, NA20348, HG00378, HG01269, HG01756, HG00345, HG01926
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620935
Frequency
Sample Size2504
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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