A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687492



Internal ID15424144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68555027..68558116hg38UCSC Ensembl
Innerchr13:69129159..69132248hg19UCSC Ensembl
Innerchr13:68027160..68030249hg18UCSC Ensembl
Innerchr13:68027160..68030249hg17UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg383090
hg193090
hg183090
hg173090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521148
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687492
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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