A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696834



Internal ID15433486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92470330..92472197hg38UCSC Ensembl
Innerchr15:93013560..93015427hg19UCSC Ensembl
Innerchr15:90814564..90816431hg18UCSC Ensembl
Innerchr15:90814564..90816431hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381868
hg191868
hg181868
hg171868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519402
Supporting Variants
Samples
Known GenesC15orf32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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