A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16920973



Internal ID14766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168042601..168052603hg38UCSC Ensembl
chr2:168899111..168909113hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3810003
hg1910003
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561251
Supporting Variants
Samples
Known GenesSTK39
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16920973
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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