A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028841



Internal ID20595881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21341017..21345286hg38UCSC Ensembl
chr16:21352338..21356607hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384270
hg194270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514830
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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