A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924781



Internal ID17267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207609176..207721927hg38UCSC Ensembl
chr2:208473900..208586651hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38112752
hg19112752
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556089
Supporting Variants
Samples
Known GenesCCNYL1, METTL21A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924781
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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