A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848138



Internal ID16142094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87256693..87320484hg38UCSC Ensembl
Innerchr15:87799924..87863715hg19UCSC Ensembl
Innerchr15:85600928..85664719hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3863792
hg1963792
hg1863792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570364
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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