A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125832



Internal ID15632332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144785726..144877525hg38UCSC Ensembl
Innerchr8:146011111..146102910hg19UCSC Ensembl
Innerchr8:145981915..146073714hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3891800
hg1991800
hg1891800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612969
Supporting Variants
Samples
Known GenesCOMMD5, MIR6850, RPL8, ZNF250, ZNF34, ZNF517, ZNF7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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