A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045201



Internal ID21954471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49236788..49237364hg38UCSC Ensembl
chr19:49740045..49740621hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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