A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517833



Internal ID15445126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84737633..84785121hg38UCSC Ensembl
Innerchr15:85280864..85328352hg19UCSC Ensembl
Innerchr15:83081868..83129356hg18UCSC Ensembl
Innerchr15:83081868..83129356hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3847489
hg1947489
hg1847489
hg1747489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695237
Samples
Known GenesZNF592
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517833
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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