A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595472



Internal ID16036195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133948569..134063406hg38UCSC Ensembl
Innerchr4:134869724..134984561hg19UCSC Ensembl
Innerchr4:135089174..135204011hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38114838
hg19114838
hg18114838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9274n54
Supporting Variantsnssv1006917, nssv1006918
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595472
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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