A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520825



Internal ID15101432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064222..31092594hg38UCSC Ensembl
Innerchr15:31356425..31384797hg19UCSC Ensembl
Innerchr15:29143717..29172089hg18UCSC Ensembl
Innerchr15:29143717..29172089hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3828373
hg1928373
hg1828373
hg1728373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676004, nssv683991, nssv684068, nssv686352
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520825
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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