A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520801



Internal ID20894162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32204211..32263952hg38UCSC Ensembl
chr19:32695117..32754858hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3859742
hg1959742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520801
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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