A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995312



Internal ID21904655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105806157..105816161hg38UCSC Ensembl
chr4:106727314..106737318hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3810005
hg1910005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553386
Samples
Known GenesGSTCD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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