A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042926



Internal ID19132145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31696725..32257538hg38UCSC Ensembl
Innerchr15:31988928..32549739hg19UCSC Ensembl
Innerchr15:29776220..30337031hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38560814
hg19560812
hg18560812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2535n100
Supporting Variantsnssv3547670
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)nsv1042926
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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