A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598506



Internal ID20971577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12810724..12811701hg38UCSC Ensembl
chr19:12921538..12922515hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245077
Samples
Known GenesRNASEH2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598506
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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