A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045238



Internal ID21954506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2433570..2433674hg38UCSC Ensembl
chr19:2433568..2433672hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624083
Samples
Known GenesLMNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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