A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523842



Internal ID20897203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1784498..1786503hg38UCSC Ensembl
chr19:1784497..1786502hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382006
hg192006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045043
Samples
Known GenesATP8B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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