A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924789



Internal ID17273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207654022..207664494hg38UCSC Ensembl
chr2:208518746..208529218hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3810473
hg1910473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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