A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596233



Internal ID16383642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173409512..173501862hg38UCSC Ensembl
Innerchr4:174330663..174423013hg19UCSC Ensembl
Innerchr4:174567238..174659588hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3892351
hg1992351
hg1892351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152851
Samples1780862127_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596233
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