A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848130



Internal ID16142086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85797294..85806589hg38UCSC Ensembl
Innerchr15:86340525..86349820hg19UCSC Ensembl
Innerchr15:84141529..84150824hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg389296
hg199296
hg189296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570355
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)nssv848130
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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