A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060391



Internal ID21969624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21750025..22771714hg38UCSC Ensembl
chr19:21932827..22954516hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381021690
hg191021690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629064
Samples
Known GenesLOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060391
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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