A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13704689



Internal ID4070592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15915712..15921767hg38UCSC Ensembl
Innerchr10:15915713..15921767hg38UCSC Ensembl
Outerchr10:15915712..15921768hg38UCSC Ensembl
chr10:15957711..15963766hg19UCSC Ensembl
Innerchr10:15957712..15963766hg19UCSC Ensembl
Outerchr10:15957711..15963767hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386056
hg196056
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622458
Supporting Variants
SamplesHG03703
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13704689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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