A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600018



Internal ID20973089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50370761..50371482hg38UCSC Ensembl
chr19:50874018..50874739hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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