A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522662



Internal ID20896023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39637056..39820842hg38UCSC Ensembl
chr19:40127696..40311482hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38183787
hg19183787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047891
Samples
Known GenesCLC, LEUTX, LGALS14, LGALS16, LGALS17A, LOC100129935
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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