A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125829



Internal ID15632329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144532947..144545017hg38UCSC Ensembl
Innerchr8:145758331..145770401hg19UCSC Ensembl
Innerchr8:145729139..145741209hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3812071
hg1912071
hg1812071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612966
Supporting Variants
Samples
Known GenesARHGAP39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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