A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596271



Internal ID16383680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178184384..178414107hg38UCSC Ensembl
Innerchr4:179105538..179335261hg19UCSC Ensembl
Innerchr4:179342532..179572255hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38229724
hg19229724
hg18229724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9406n54
Supporting Variantsnssv1017038
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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