A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848193



Internal ID16142149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87287915..87346519hg38UCSC Ensembl
Innerchr15:87831146..87889750hg19UCSC Ensembl
Innerchr15:85632150..85690754hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3858605
hg1958605
hg1858605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570379
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)nssv848193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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