A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043845



Internal ID19133064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87274799..87327490hg38UCSC Ensembl
Innerchr15:87818030..87870721hg19UCSC Ensembl
Innerchr15:85619034..85671725hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3852692
hg1952692
hg1852692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2654n100
Supporting Variantsnssv3555101, nssv3718152
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)nsv1043845
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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