A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125567



Internal ID15632067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143616728..143624968hg38UCSC Ensembl
Innerchr8:144698898..144707138hg19UCSC Ensembl
Innerchr8:144770041..144778281hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg388241
hg198241
hg188241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612858
Supporting Variants
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125567
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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