A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705098



Internal ID15441750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54864770..55028267hg38UCSC Ensembl
Innerchr13:55438905..55602402hg19UCSC Ensembl
Innerchr13:54336906..54500403hg18UCSC Ensembl
Innerchr13:54336906..54500403hg17UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38163498
hg19163498
hg18163498
hg17163498
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528493
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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