A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518064



Internal ID15098671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85178426..85605928hg38UCSC Ensembl
Innerchr15:85721657..86149159hg19UCSC Ensembl
Innerchr15:83522661..83950163hg18UCSC Ensembl
Innerchr15:83522661..83950163hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38427503
hg19427503
hg18427503
hg17427503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694197
Samples
Known GenesAKAP13, LOC440300, LOC642423
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518064
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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