A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596607



Internal ID20969678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37223739..37225099hg38UCSC Ensembl
chr19:37714641..37716001hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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