A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699941



Internal ID15089907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56961324..56963321hg38UCSC Ensembl
Innerchr16:56995236..56997233hg19UCSC Ensembl
Innerchr16:55552737..55554734hg18UCSC Ensembl
Innerchr16:55552737..55554734hg17UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381998
hg191998
hg181998
hg171998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524073
Supporting Variants
Samples
Known GenesCETP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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