A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249114



Internal ID20816154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57824107..58014702hg38UCSC Ensembl
chr19:58335475..58526070hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38190596
hg19190596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595588
Supporting Variants
Samples
Known GenesC19orf18, FKBP1AP1, LOC100128398, ZNF256, ZNF417, ZNF418, ZNF587, ZNF587B, ZNF606, ZNF814
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01112


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