A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980669



Internal ID21890012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110080400..110083108hg38UCSC Ensembl
chr1:110623022..110625730hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382709
hg192709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980669
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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