A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598693



Internal ID20971764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16479954..16481594hg38UCSC Ensembl
chr19:16590765..16592405hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247554
Samples
Known GenesCALR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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