A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125289



Internal ID15978475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143491941..143549816hg38UCSC Ensembl
Innerchr8:144574111..144631986hg19UCSC Ensembl
Innerchr8:144645254..144703129hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3857876
hg1957876
hg1857876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612775
Supporting Variants
Samples
Known GenesZC3H3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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