A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038072



Internal ID19127291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32285928hg38UCSC Ensembl
Innerchr15:32458661..32578129hg19UCSC Ensembl
Innerchr15:30245953..30365421hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38119469
hg19119469
hg18119469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2539n100
Supporting Variantsnssv3721610
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)nsv1038072
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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