A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517207



Internal ID15097814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69711242..69738011hg38UCSC Ensembl
Innerchr16:69745145..69771914hg19UCSC Ensembl
Innerchr16:68302646..68329415hg18UCSC Ensembl
Innerchr16:68302646..68329415hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3826770
hg1926770
hg1826770
hg1726770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662557, nssv653708, nssv683447, nssv663543
Samples
Known GenesNQO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517207
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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