A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926775



Internal ID18580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167025618..167085618hg38UCSC Ensembl
chr2:167882128..167942128hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3860001
hg1960001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446366
Supporting Variants
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000469


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