A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003640



Internal ID16297596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102860860..102861806hg38UCSC Ensembl
Innerchr4:103782017..103782963hg19UCSC Ensembl
Innerchr4:104001106..104002052hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38947
hg19947
hg18947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594973
Supporting Variants
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1003640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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