A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520766



Internal ID15448059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112732761..112742949hg38UCSC Ensembl
Innerchr4:113653917..113664105hg19UCSC Ensembl
Innerchr4:113873366..113883554hg18UCSC Ensembl
Innerchr4:114011521..114021709hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3810189
hg1910189
hg1810189
hg1710189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675129, nssv688371
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520766
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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