A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245610



Internal ID20812650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23467269..23882455hg38UCSC Ensembl
chr19:23650071..24065257hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38415187
hg19415187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598216
Supporting Variants
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245610
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00019


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