A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690037



Internal ID15426689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24821213..24833640hg38UCSC Ensembl
Innerchr15:25066360..25078787hg19UCSC Ensembl
Innerchr15:22617453..22629880hg18UCSC Ensembl
Innerchr15:22617453..22629880hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3812428
hg1912428
hg1812428
hg1712428
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515875
Supporting Variants
Samples
Known GenesSNRPN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690037
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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