A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686102



Internal ID15076068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32218309..32222725hg38UCSC Ensembl
Innerchr15:32510510..32514926hg19UCSC Ensembl
Innerchr15:30297802..30302218hg18UCSC Ensembl
Innerchr15:30297802..30302218hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg384417
hg194417
hg184417
hg174417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517740
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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