A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596313



Internal ID20969384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23405769..23771164hg38UCSC Ensembl
chr19:23588571..23953966hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38365396
hg19365396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3487n223
Supporting Variantsnssv18245606
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596313
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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