A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882686



Internal ID22657663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123090175..123846417hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38756243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882686
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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