A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663543



Internal ID15053509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69723925..69738011hg38UCSC Ensembl
Innerchr16:69757828..69771914hg19UCSC Ensembl
Innerchr16:68315329..68329415hg18UCSC Ensembl
Innerchr16:68315329..68329415hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3814087
hg1914087
hg1814087
hg1714087
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517207
Supporting Variants
Samples
Known GenesNQO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663543
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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