A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516577



Internal ID15443870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152945141..152980934hg38UCSC Ensembl
Innerchr5:152324701..152360494hg19UCSC Ensembl
Innerchr5:152304894..152340687hg18UCSC Ensembl
Innerchr5:152304894..152340687hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3835794
hg1935794
hg1835794
hg1735794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693296, nssv674547, nssv674596, nssv669285, nssv699917, nssv676759, nssv701385, nssv675610
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516577
Frequency
Sample Size2026
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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