A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683002



Internal ID15072968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31736601..32151995hg38UCSC Ensembl
Innerchr15:32028804..32444196hg19UCSC Ensembl
Innerchr15:29816096..30231488hg18UCSC Ensembl
Innerchr15:29816096..30231488hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38415395
hg19415393
hg18415393
hg17415393
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)nssv683002
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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