A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921326



Internal ID14984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159316539..159936193hg38UCSC Ensembl
chr2:160173050..160792704hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38619655
hg19619655
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560575
Supporting Variants
Samples
Known GenesBAZ2B, CD302, LY75, LY75-CD302, MARCH7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921326
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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