A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052979



Internal ID19142198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32323088hg38UCSC Ensembl
Innerchr15:32458661..32615289hg19UCSC Ensembl
Innerchr15:30245953..30402581hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38156629
hg19156629
hg18156629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2540n100
Supporting Variantsnssv3547725
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)nsv1052979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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