A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595427



Internal ID16382836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131433132hg38UCSC Ensembl
Innerchr4:131946375..132354287hg19UCSC Ensembl
Innerchr4:132165825..132573737hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38407913
hg19407913
hg18407913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9266n54
Supporting Variantsnssv1006494
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595427
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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