A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558284



Internal ID331353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40171920..40325062hg38UCSC Ensembl
chr19:40677827..40830969hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38153143
hg19153143
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723384
Samples
Known GenesAKT2, C19orf47, CNTD2, MAP3K10, MIR641, TTC9B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558284
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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