A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521833



Internal ID15102440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77482366..77785544hg38UCSC Ensembl
Innerchr16:77516263..77819441hg19UCSC Ensembl
Innerchr16:76073764..76376942hg18UCSC Ensembl
Innerchr16:76073764..76376942hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38303179
hg19303179
hg18303179
hg17303179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694606
Samples
Known GenesNUDT7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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