A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031696



Internal ID20598736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68331930..68332367hg38UCSC Ensembl
chr16:68365833..68366270hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510849
Supporting Variants
Samples
Known GenesPRMT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00053


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