A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922935



Internal ID16046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203462846..203462919hg38UCSC Ensembl
chr2:204327569..204327642hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453071
Supporting Variants
Samples
Known GenesRAPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922935
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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