A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756703



Internal ID3797608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36909639..37046972hg38UCSC Ensembl
Innerchr10:36910139..37046472hg38UCSC Ensembl
Outerchr10:36908639..37047972hg38UCSC Ensembl
chr10:37198567..37335900hg19UCSC Ensembl
Innerchr10:37199067..37335400hg19UCSC Ensembl
Outerchr10:37197567..37336900hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38137334
hg19137334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622939
Supporting Variants
SamplesHG03445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756703
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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