A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985234



Internal ID21894577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92978771..92979953hg38UCSC Ensembl
chr1:93444328..93445510hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381183
hg191183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985234
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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