A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690340



Internal ID6671816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8508475..8518369hg38UCSC Ensembl
Innerchr10:8508975..8517869hg38UCSC Ensembl
Outerchr10:8507475..8519369hg38UCSC Ensembl
chr10:8550438..8560332hg19UCSC Ensembl
Innerchr10:8550938..8559832hg19UCSC Ensembl
Outerchr10:8549438..8561332hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389895
hg199895
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622287
Supporting Variants
SamplesNA20810
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690340
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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