A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16917253



Internal ID12246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:110100675..110101070hg38UCSC Ensembl
chr2:110858252..110858647hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559005
Supporting Variants
Samples
Known GenesMALL
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16917253
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001405


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