A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668218



Internal ID15404870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18601360..18665393hg38UCSC Ensembl
Innerchr5:18601469..18665502hg19UCSC Ensembl
Innerchr5:18637226..18701259hg18UCSC Ensembl
Innerchr5:18637226..18701259hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3864034
hg1964034
hg1864034
hg1764034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516047
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668218
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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