A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526817



Internal ID15454110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5181445..5183670hg38UCSC Ensembl
Innerchr5:5181558..5183783hg19UCSC Ensembl
Innerchr5:5234558..5236783hg18UCSC Ensembl
Innerchr5:5234558..5236783hg17UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382226
hg192226
hg182226
hg172226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703171
Samples
Known GenesADAMTS16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526817
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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