A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031728



Internal ID20598768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68724838..68728397hg38UCSC Ensembl
chr16:68758741..68762300hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383560
hg193560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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