A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612775



Internal ID16400184
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 StatusM
Merged Variantsdgv12409n54
Supporting Variantsnssv1125289
Samples
Known GenesZC3H3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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