A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705178



Internal ID15441830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:32978544..32979411hg38UCSC Ensembl
Innerchr13:33552682..33553549hg19UCSC Ensembl
Innerchr13:32450682..32451549hg18UCSC Ensembl
Innerchr13:32450682..32451549hg17UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38868
hg19868
hg18868
hg17868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528562
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705178
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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