A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533369



Internal ID20906730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55502943..55504721hg38UCSC Ensembl
chr19:56014310..56016088hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381779
hg191779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199633
Samples
Known GenesSSC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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