A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679151



Internal ID15415803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95279738..95331133hg38UCSC Ensembl
Innerchr13:95931992..95983387hg19UCSC Ensembl
Innerchr13:94729993..94781388hg18UCSC Ensembl
Innerchr13:94729993..94781388hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3851396
hg1951396
hg1851396
hg1751396
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)nssv679151
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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