A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694350



Internal ID15084316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61882935..62008895hg38UCSC Ensembl
Innerchr15:62175134..62301094hg19UCSC Ensembl
Innerchr15:59962426..60088386hg18UCSC Ensembl
Innerchr15:59962426..60088386hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38125961
hg19125961
hg18125961
hg17125961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516639
Supporting Variants
Samples
Known GenesVPS13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694350
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer