A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547671



Internal ID18845952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31696725..32329014hg38UCSC Ensembl
Innerchr15:31988928..32621215hg19UCSC Ensembl
Innerchr15:29776220..30408507hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38632290
hg19632288
hg18632288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036819
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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