A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993125



Internal ID21902468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37007799..37007905hg38UCSC Ensembl
chr3:37049290..37049396hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542129
Samples
Known GenesMLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993125
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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