A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195300



Internal ID20762340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76608706..77690545hg38UCSC Ensembl
chr16:76642603..77724442hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381081840
hg191081840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498681
Supporting Variants
Samples
Known GenesADAMTS18, MIR4719, MON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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