A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522661



Internal ID20896022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57761472..57777007hg38UCSC Ensembl
chr19:58272840..58288375hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3815536
hg1915536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199715
Samples
Known GenesZNF586
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522661
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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