A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597315



Internal ID20970386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23616131..23893811hg38UCSC Ensembl
chr19:23798933..24076613hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38277681
hg19277681
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245618
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597315
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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