A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695193



Internal ID15085159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34661785..35170780hg38UCSC Ensembl
Innerchr15:34953986..35462981hg19UCSC Ensembl
Innerchr15:32741278..33250273hg18UCSC Ensembl
Innerchr15:32741278..33250273hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38508996
hg19508996
hg18508996
hg17508996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522411
Supporting Variants
Samples
Known GenesACTC1, AQR, GJD2, ZNF770
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695193
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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