A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922893



Internal ID16021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202200910..202202025hg38UCSC Ensembl
chr2:203065633..203066748hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922893
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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