A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558329



Internal ID331395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199944381..199944411hg38UCSC Ensembl
chr2:200809104..200809134hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3831
hg1931
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16927848
Samples
Known GenesTYW5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558329
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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