A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059790



Internal ID21969023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43512440..43514780hg38UCSC Ensembl
chr19:44016592..44018932hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg382341
hg192341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626254
Samples
Known GenesETHE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059790
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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