A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547669



Internal ID18845950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31696725..32247324hg38UCSC Ensembl
Innerchr15:31988928..32539525hg19UCSC Ensembl
Innerchr15:29776220..30326817hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38550600
hg19550598
hg18550598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050183
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)nssv3547669
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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