A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524495



Internal ID15451788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163110385..163123720hg38UCSC Ensembl
Innerchr5:162537391..162550726hg19UCSC Ensembl
Innerchr5:162469969..162483304hg18UCSC Ensembl
Innerchr5:162469969..162483304hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3813336
hg1913336
hg1813336
hg1713336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700433
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524495
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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