A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657607



Internal ID15394259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11436705..11437771hg38UCSC Ensembl
Innerchr10:11478704..11479770hg19UCSC Ensembl
Innerchr10:11518710..11519776hg18UCSC Ensembl
Innerchr10:11518710..11519776hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381067
hg191067
hg181067
hg171067
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515865
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657607
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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