A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106253



Internal ID15612753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10474126..10629142hg38UCSC Ensembl
Innerchr8:10331636..10486652hg19UCSC Ensembl
Innerchr8:10369046..10524062hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38155017
hg19155017
hg18155017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610268
Supporting Variants
Samples
Known GenesPRSS55, RP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106253
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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