A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053950



Internal ID19143169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31696725..32144319hg38UCSC Ensembl
Innerchr15:31988928..32436520hg19UCSC Ensembl
Innerchr15:29776220..30223812hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38447595
hg19447593
hg18447593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2536n100
Supporting Variantsnssv3547665
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)nsv1053950
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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