A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593307



Internal ID16034030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1517595..1594238hg38UCSC Ensembl
Innerchr4:1519322..1595965hg19UCSC Ensembl
Innerchr4:1488616..1565924hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3876644
hg1976644
hg1877309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8895n54
Supporting Variantsnssv987695
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593307
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