A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986424



Internal ID21895767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135860040..135860370hg38UCSC Ensembl
chr2:136617610..136617940hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537521
Samples
Known GenesMCM6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986424
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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