A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984891



Internal ID21894234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62762495..62762627hg38UCSC Ensembl
chr1:63228166..63228298hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984891
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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