A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982799



Internal ID21892142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218909034..218915360hg38UCSC Ensembl
chr1:219082376..219088702hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg386327
hg196327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982799
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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