A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922974



Internal ID16071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206105807..206106353hg38UCSC Ensembl
chr2:206970531..206971077hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922974
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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