A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246292



Internal ID20813332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41749358..42444703hg38UCSC Ensembl
chr19:42253266..42948855hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38695346
hg19695590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596591
Supporting Variants
Samples
Known GenesARHGEF1, ATP1A3, CD79A, CEACAM3, CEACAM6, CIC, CNFN, CXCL17, DEDD2, DMRTC2, ERF, GRIK5, GSK3A, LIPE, LIPE-AS1, LOC100505622, LYPD4, MEGF8, MIR4323, MIR6797, MIR8077, PAFAH1B3, POU2F2, PRR19, RABAC1, RPS19, TMEM145, ZNF526, ZNF574
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00323


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