A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596264



Internal ID16383673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176417484..176435081hg38UCSC Ensembl
Innerchr4:177338635..177356232hg19UCSC Ensembl
Innerchr4:177575629..177593226hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3817598
hg1917598
hg1817598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9404n54
Supporting Variantsnssv1017030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596264
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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