A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998697



Internal ID19158233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25590273hg38UCSC Ensembl
Innerchr4:25557047..25591895hg19UCSC Ensembl
Innerchr4:25166145..25200993hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3834849
hg1934849
hg1834849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5160n100
Supporting Variantsnssv3620608, nssv3620607
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)nsv998697
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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