A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028851



Internal ID20595891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21644871..21645587hg38UCSC Ensembl
chr16:21656192..21656908hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508386
Supporting Variants
Samples
Known GenesIGSF6, METTL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028851
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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