A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125836



Internal ID15979022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144970446..145049322hg38UCSC Ensembl
Innerchr8:146195832..146274708hg19UCSC Ensembl
Innerchr8:146166636..146245512hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3878877
hg1978877
hg1878877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612973
Supporting Variants
Samples
Known GenesTMED10P1, ZNF252P, ZNF252P-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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