A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926783



Internal ID18587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167120350..167169476hg38UCSC Ensembl
chr2:167976860..168025986hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3849127
hg1949127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434340
Supporting Variants
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926783
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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