A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595604



Internal ID20968675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12810782..12812771hg38UCSC Ensembl
chr19:12921596..12923585hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245078
Samples
Known GenesRNASEH2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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