A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046672



Internal ID19135891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23836999..23892763hg38UCSC Ensembl
Innerchr15:24082146..24137910hg19UCSC Ensembl
Innerchr15:21633239..21689003hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3855765
hg1955765
hg1855765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3538950
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)nsv1046672
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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