A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687984



Internal ID15424636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95348742..95383629hg38UCSC Ensembl
Innerchr13:96000996..96035883hg19UCSC Ensembl
Innerchr13:94798997..94833884hg18UCSC Ensembl
Innerchr13:94798997..94833884hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3834888
hg1934888
hg1834888
hg1734888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517610
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687984
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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