A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529779



Internal ID20903140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46445192..46449093hg38UCSC Ensembl
chr19:46948449..46952350hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529779
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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