A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059836



Internal ID21969069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35793748..35794471hg38UCSC Ensembl
chr19:36284650..36285373hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619896
Samples
Known GenesLOC644050
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059836
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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