A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558879



Internal ID331931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:151769884..151771397hg38UCSC Ensembl
chr2:152626398..152627911hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16925503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558879
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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