A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044429



Internal ID19133648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31736552..32387416hg38UCSC Ensembl
Innerchr15:32028755..32679617hg19UCSC Ensembl
Innerchr15:29816047..30466909hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38650865
hg19650863
hg18650863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2535n100
Supporting Variantsnssv3547710
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)nsv1044429
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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