A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997582



Internal ID21906925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56527890..56539470hg38UCSC Ensembl
chr4:57394056..57405636hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3811581
hg1911581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547146
Samples
Known GenesTHEGL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997582
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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