A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031913



Internal ID20598953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70621101..70624100hg38UCSC Ensembl
chr16:70655004..70658003hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505675
Supporting Variants
Samples
Known GenesIL34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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