A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923067



Internal ID16136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210940686..210940766hg38UCSC Ensembl
chr2:211805410..211805490hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450586
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923067
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.014678


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