A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045116



Internal ID19134335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67842689..67863372hg38UCSC Ensembl
Innerchr15:68135027..68155710hg19UCSC Ensembl
Innerchr15:65922081..65942764hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3820684
hg1920684
hg1820684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553652
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)nsv1045116
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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