A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517816



Internal ID15445109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:175196080..175209574hg38UCSC Ensembl
Innerchr5:174623083..174636577hg19UCSC Ensembl
Innerchr5:174555689..174569183hg18UCSC Ensembl
Innerchr5:174555689..174569183hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3813495
hg1913495
hg1813495
hg1713495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695221
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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