A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055758



Internal ID21964991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34405605..34405692hg38UCSC Ensembl
chr19:34896510..34896597hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624002
Samples
Known GenesPDCD2L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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