A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527990



Internal ID15455283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69152867..69159339hg38UCSC Ensembl
Innerchr5:68448694..68455166hg19UCSC Ensembl
Innerchr5:68484450..68490922hg18UCSC Ensembl
Innerchr5:68484450..68490922hg17UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg386473
hg196473
hg186473
hg176473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704513
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527990
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