A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246716



Internal ID20813756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52690073..53366193hg38UCSC Ensembl
chr19:53193326..53869446hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38676121
hg19676121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596246
Supporting Variants
Samples
Known GenesBIRC8, ERVV-1, ERVV-2, FAM90A27P, VN1R2, VN1R4, ZNF160, ZNF28, ZNF320, ZNF321P, ZNF347, ZNF415, ZNF468, ZNF525, ZNF600, ZNF611, ZNF665, ZNF677, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF818P, ZNF83, ZNF845
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246716
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.21986


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