A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702216



Internal ID15092182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21593859..21677423hg38UCSC Ensembl
Innerchr16:21605180..21688744hg19UCSC Ensembl
Innerchr16:21512681..21596245hg18UCSC Ensembl
Innerchr16:21512681..21596245hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3883565
hg1983565
hg1883565
hg1783565
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517713
Supporting Variants
Samples
Known GenesIGSF6, METTL9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702216
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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