A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527672



Internal ID15454965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53760061..53771034hg38UCSC Ensembl
Innerchr4:54626228..54637201hg19UCSC Ensembl
Innerchr4:54320985..54331958hg18UCSC Ensembl
Innerchr4:54467156..54478129hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3810974
hg1910974
hg1810974
hg1710974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704147
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527672
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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