A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595593



Internal ID16383002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139628325..139657888hg38UCSC Ensembl
Innerchr4:140549479..140579042hg19UCSC Ensembl
Innerchr4:140768929..140798492hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3829564
hg1929564
hg1829564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008229
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595593
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