A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612073



Internal ID16399482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119143352..119153018hg38UCSC Ensembl
Innerchr8:120155591..120165257hg19UCSC Ensembl
Innerchr8:120224772..120234438hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg389667
hg199667
hg189667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12297n54
Supporting Variantsnssv1120257, nssv1120263, nssv1120256, nssv1120259, nssv1120262, nssv1120261, nssv1120258, nssv1120260
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612073
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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