A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848952



Internal ID16142908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93658699..93742016hg38UCSC Ensembl
Innerchr15:94201928..94285245hg19UCSC Ensembl
Innerchr15:92002932..92086249hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3883318
hg1983318
hg1883318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570525
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)nssv848952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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