A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519999



Internal ID15100606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68931952..69015325hg38UCSC Ensembl
Innerchr10:70691708..70775081hg19UCSC Ensembl
Innerchr10:70361714..70445087hg18UCSC Ensembl
Innerchr10:70361714..70445087hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3883374
hg1983374
hg1883374
hg1783374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677258, nssv660009, nssv685613
Samples
Known GenesDDX21, DDX50, KIAA1279
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519999
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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