A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715691



Internal ID19013972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19998696hg38UCSC Ensembl
Innerchr15:20016316..20203949hg19UCSC Ensembl
Innerchr15:18276329..18463963hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38187634
hg19187634
hg18187635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036442
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3715691
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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