A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703554



Internal ID15093520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56973280..56973441hg38UCSC Ensembl
Innerchr16:57007192..57007353hg19UCSC Ensembl
Innerchr16:55564693..55564854hg18UCSC Ensembl
Innerchr16:55564693..55564854hg17UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38162
hg19162
hg18162
hg17162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527160
Supporting Variants
Samples
Known GenesCETP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703554
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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