A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593490



Internal ID16380899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5733576..5777590hg38UCSC Ensembl
Innerchr4:5735303..5779317hg19UCSC Ensembl
Innerchr4:5786204..5830218hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3844015
hg1944015
hg1844015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8932n54
Supporting Variantsnssv989315
Samples
Known GenesEVC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593490
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