A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662882



Internal ID15052848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31728323..32222140hg38UCSC Ensembl
Innerchr15:32020526..32514341hg19UCSC Ensembl
Innerchr15:29807818..30301633hg18UCSC Ensembl
Innerchr15:29807818..30301633hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38493818
hg19493816
hg18493816
hg17493816
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)nssv662882
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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