A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636159



Internal ID18934440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159452069..159473983hg38UCSC Ensembl
Innerchr4:160373221..160395135hg19UCSC Ensembl
Innerchr4:160592671..160614585hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3821915
hg1921915
hg1821915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024453
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636159
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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