A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535080



Internal ID20908441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38979013..38979532hg38UCSC Ensembl
chr19:39469653..39470172hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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