A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525720



Internal ID15453013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186871511..187504975hg38UCSC Ensembl
Innerchr4:187792665..188426129hg19UCSC Ensembl
Innerchr4:188029659..188663123hg18UCSC Ensembl
Innerchr4:188167814..188801278hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38633465
hg19633465
hg18633465
hg17633465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701883
Samples
Known GenesLOC339975
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525720
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