A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985169



Internal ID21894512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76774377..76774454hg38UCSC Ensembl
chr1:77240062..77240139hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985169
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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