A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995488



Internal ID21904831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153724973..153725055hg38UCSC Ensembl
chr4:154646125..154646207hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547556
Samples
Known GenesRNF175
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995488
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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