A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984335



Internal ID21893678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41527052..41527136hg38UCSC Ensembl
chr1:41992723..41992807hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534539
Samples
Known GenesHIVEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984335
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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