A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693373



Internal ID15430025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95290238..95383629hg38UCSC Ensembl
Innerchr13:95942492..96035883hg19UCSC Ensembl
Innerchr13:94740493..94833884hg18UCSC Ensembl
Innerchr13:94740493..94833884hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3893392
hg1993392
hg1893392
hg1793392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517610
Supporting Variants
Samples
Known GenesABCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693373
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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