A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13695985



Internal ID3697801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11478380..11480469hg38UCSC Ensembl
Innerchr10:11478383..11480466hg38UCSC Ensembl
Outerchr10:11478377..11480472hg38UCSC Ensembl
chr10:11520379..11522468hg19UCSC Ensembl
Innerchr10:11520382..11522465hg19UCSC Ensembl
Outerchr10:11520376..11522471hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622339
Supporting Variants
SamplesNA18994
Known GenesUSP6NL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13695985
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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