A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723531



Internal ID147197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41797706..42527281hg38UCSC Ensembl
chr19:42301638..43031433hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38729576
hg19729796
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562413
Supporting Variants
Samples
Known GenesARHGEF1, ATP1A3, CD79A, CEACAM1, CEACAM3, 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
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723531
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.044958


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