A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697915



Internal ID15434567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43994966..43995084hg38UCSC Ensembl
Innerchr10:44490414..44490532hg19UCSC Ensembl
Innerchr10:43810420..43810538hg18UCSC Ensembl
Innerchr10:43810420..43810538hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38119
hg19119
hg18119
hg17119
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521308
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697915
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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