A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004158



Internal ID19093375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65709330..65740812hg38UCSC Ensembl
Innerchr4:66575048..66606530hg19UCSC Ensembl
Innerchr4:66257643..66289125hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3831483
hg1931483
hg1831483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5237n100
Supporting Variantsnssv3740173
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)nsv1004158
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