A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003619



Internal ID16297575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102859683..102861607hg38UCSC Ensembl
Innerchr4:103780840..103782764hg19UCSC Ensembl
Innerchr4:103999940..104001853hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381925
hg191925
hg181914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594963
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)nssv1003619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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