A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517488



Internal ID15444781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:760039..810673hg38UCSC Ensembl
Innerchr16:810039..860673hg19UCSC Ensembl
Innerchr16:750040..800674hg18UCSC Ensembl
Innerchr16:750040..800674hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850635
hg1950635
hg1850635
hg1750635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652170, nssv676853
Samples
Known GenesCHTF18, GNG13, MIR662, MSLN, PRR25, RPUSD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517488
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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