A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996780



Internal ID21906123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181975577..181975729hg38UCSC Ensembl
chr4:182896730..182896882hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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