A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520408



Internal ID15101015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78117849..78137411hg38UCSC Ensembl
Innerchr16:78151746..78171308hg19UCSC Ensembl
Innerchr16:76709247..76728809hg18UCSC Ensembl
Innerchr16:76709247..76728809hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3819563
hg1919563
hg1819563
hg1719563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680768, nssv671227
Samples
Known GenesWWOX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520408
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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