A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595694



Internal ID20968765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40010167..40010801hg38UCSC Ensembl
chr19:40516074..40516708hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248405
Samples
Known GenesZNF546
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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