A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926767



Internal ID18573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166940443..166942065hg38UCSC Ensembl
chr2:167796953..167798575hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450832
Supporting Variants
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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