A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681056



Internal ID15071022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31736601..32222725hg38UCSC Ensembl
Innerchr15:32028804..32514926hg19UCSC Ensembl
Innerchr15:29816096..30302218hg18UCSC Ensembl
Innerchr15:29816096..30302218hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38486125
hg19486123
hg18486123
hg17486123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517740
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681056
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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