A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666339



Internal ID15056305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32219354..32633875hg38UCSC Ensembl
Innerchr15:32511555..32926076hg19UCSC Ensembl
Innerchr15:30298847..30713368hg18UCSC Ensembl
Innerchr15:30298847..30713368hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38414522
hg19414522
hg18414522
hg17414522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517740
Supporting Variants
Samples
Known GenesARHGAP11A, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666339
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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