A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694197



Internal ID15084163
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 StatusS
Merged Variantsnsv518064
Supporting Variants
Samples
Known GenesAKAP13, LOC440300, LOC642423
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694197
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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