A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982291



Internal ID21891634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207119712..207119793hg38UCSC Ensembl
chr1:207293057..207293138hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535914
Samples
Known GenesC4BPA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982291
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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