A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520964



Internal ID15101571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69424697..69501614hg38UCSC Ensembl
Innerchr15:69717036..69793953hg19UCSC Ensembl
Innerchr15:67504090..67581007hg18UCSC Ensembl
Innerchr15:67504090..67581007hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3876918
hg1976918
hg1876918
hg1776918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697711
Samples
Known GenesKIF23, RPLP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520964
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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