A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593495



Internal ID16034218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6232163..6300792hg38UCSC Ensembl
Innerchr4:6233890..6302519hg19UCSC Ensembl
Innerchr4:6284791..6353420hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3868630
hg1968630
hg1868630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152593
SamplesHGDP00841
Known GenesLOC285484, WFS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593495
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