A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982944



Internal ID21892287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23642544..23642850hg38UCSC Ensembl
chr1:23969034..23969340hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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