A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040969



Internal ID19130188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31719274..32149432hg38UCSC Ensembl
Innerchr15:32011477..32441633hg19UCSC Ensembl
Innerchr15:29798769..30228925hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38430159
hg19430157
hg18430157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2536n100
Supporting Variantsnssv3547674
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)nsv1040969
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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