A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657860



Internal ID15047826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31728323..32149432hg38UCSC Ensembl
Innerchr15:32020526..32441633hg19UCSC Ensembl
Innerchr15:29807818..30228925hg18UCSC Ensembl
Innerchr15:29807818..30228925hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38421110
hg19421108
hg18421108
hg17421108
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)nssv657860
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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