A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125742



Internal ID15978928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143904439..144007080hg38UCSC Ensembl
Innerchr8:144978607..145081248hg19UCSC Ensembl
Innerchr8:145050595..145153236hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38102642
hg19102642
hg18102642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612902
Supporting Variants
Samples
Known GenesGRINA, MIR661, PARP10, PLEC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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