A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988434



Internal ID15935704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1601314..1622987hg38UCSC Ensembl
Innerchr4:1603041..1624714hg19UCSC Ensembl
Innerchr4:1573001..1594673hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3821674
hg1921674
hg1821673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593332
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988434
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer