A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691437



Internal ID15081403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36274050..36290412hg38UCSC Ensembl
Innerchr13:36848187..36864549hg19UCSC Ensembl
Innerchr13:35746187..35762549hg18UCSC Ensembl
Innerchr13:35746187..35762549hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3816363
hg1916363
hg1816363
hg1716363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515635
Supporting Variants
Samples
Known GenesCCDC169, CCDC169-SOHLH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691437
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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