A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031312



Internal ID20598352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66789290..66789624hg38UCSC Ensembl
chr16:66823193..66823527hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503179
Supporting Variants
Samples
Known GenesCCDC79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.61083


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