A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526551



Internal ID15453844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:173262829..173265324hg38UCSC Ensembl
Innerchr5:172689832..172692327hg19UCSC Ensembl
Innerchr5:172622438..172624933hg18UCSC Ensembl
Innerchr5:172622438..172624933hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg382496
hg192496
hg182496
hg172496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702865
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526551
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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