A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594958



Internal ID16382367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102859340..102861164hg38UCSC Ensembl
Innerchr4:103780497..103782321hg19UCSC Ensembl
Innerchr4:103999596..104001410hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381825
hg191825
hg181815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9182n54
Supporting Variantsnssv1003604
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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