A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13851572



Internal ID2792802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68852320..68864024hg38UCSC Ensembl
Innerchr10:68852366..68863979hg38UCSC Ensembl
Outerchr10:68852275..68864070hg38UCSC Ensembl
chr10:70612076..70623780hg19UCSC Ensembl
Innerchr10:70612122..70623735hg19UCSC Ensembl
Outerchr10:70612031..70623826hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3811705
hg1911705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623730
Supporting Variants
SamplesHG02465
Known GenesSTOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13851572
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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