A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16919122



Internal ID13512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:126048809..126298175hg38UCSC Ensembl
chr2:126806386..127055752hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38249367
hg19249367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16919122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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