A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125796



Internal ID15632296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144416180..144451628hg38UCSC Ensembl
Innerchr8:145641564..145677011hg19UCSC Ensembl
Innerchr8:145612372..145647819hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3835449
hg1935448
hg1835448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612935
Supporting Variants
Samples
Known GenesCYHR1, LOC100287098, MIR6893, SLC39A4, TONSL, VPS28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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