A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517972



Internal ID20891333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:857355..865581hg38UCSC Ensembl
chr19:857355..865581hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388227
hg198227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199072
Samples
Known GenesCFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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