A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046020



Internal ID21955272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19257433..19257490hg38UCSC Ensembl
chr19:19368242..19368299hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628874
Samples
Known GenesHAPLN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046020
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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