A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698902



Internal ID15088868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77193283..77195760hg38UCSC Ensembl
Innerchr16:77227180..77229657hg19UCSC Ensembl
Innerchr16:75784681..75787158hg18UCSC Ensembl
Innerchr16:75784681..75787158hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg382478
hg192478
hg182478
hg172478
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523187
Supporting Variants
Samples
Known GenesMON1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698902
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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