A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594977



Internal ID16382386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102860969..102862255hg38UCSC Ensembl
Innerchr4:103782126..103783412hg19UCSC Ensembl
Innerchr4:104001215..104002501hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381287
hg191287
hg181287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9185n54
Supporting Variantsnssv1003645
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer