A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701559



Internal ID15091525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36263937..36290412hg38UCSC Ensembl
Innerchr13:36838074..36864549hg19UCSC Ensembl
Innerchr13:35736074..35762549hg18UCSC Ensembl
Innerchr13:35736074..35762549hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3826476
hg1926476
hg1826476
hg1726476
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525432
Supporting Variants
Samples
Known GenesCCDC169, CCDC169-SOHLH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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