A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556089



Internal ID329235
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 StatusM
Merged Variants
Supporting Variantsnssv16924781
Samples
Known GenesCCNYL1, METTL21A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556089
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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