A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527271



Internal ID15454564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110008155..110065710hg38UCSC Ensembl
Innerchr5:109343856..109401411hg19UCSC Ensembl
Innerchr5:109371755..109429310hg18UCSC Ensembl
Innerchr5:109371755..109429310hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3857556
hg1957556
hg1857556
hg1757556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703681
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527271
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