A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515971



Internal ID20889332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:823062..826081hg38UCSC Ensembl
chr19:823062..826081hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383020
hg193020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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