A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658969



Internal ID15395621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43023729..43024055hg38UCSC Ensembl
Innerchr13:43597865..43598191hg19UCSC Ensembl
Innerchr13:42495865..42496191hg18UCSC Ensembl
Innerchr13:42495865..42496191hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38327
hg19327
hg18327
hg17327
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519830
Supporting Variants
Samples
Known GenesDNAJC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658969
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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