A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518937



Internal ID20892298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53514552..53529647hg38UCSC Ensembl
chr19:54017806..54032901hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815096
hg1915096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200191
Samples
Known GenesZNF331
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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