A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517916



Internal ID20891277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39323861..39325320hg38UCSC Ensembl
chr19:39814501..39815960hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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