A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13751194



Internal ID4521461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32939123..32950883hg38UCSC Ensembl
Innerchr10:32939123..32950883hg38UCSC Ensembl
Outerchr10:32938623..32951383hg38UCSC Ensembl
chr10:33228051..33239811hg19UCSC Ensembl
Innerchr10:33228051..33239811hg19UCSC Ensembl
Outerchr10:33227551..33240311hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811761
hg1911761
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622842
Supporting Variants
SamplesHG04019
Known GenesITGB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13751194
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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