A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594960



Internal ID16382369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102859340..102861607hg38UCSC Ensembl
Innerchr4:103780497..103782764hg19UCSC Ensembl
Innerchr4:103999596..104001853hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382268
hg192268
hg182258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9182n54
Supporting Variantsnssv1003607, nssv1003610, nssv1003608, nssv1003609, nssv1003606
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594960
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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