A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561320



Internal ID334303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207223645..207231407hg38UCSC Ensembl
chr2:208088369..208096131hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg387763
hg197763
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561320
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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