A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556725



Internal ID329856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5658847..5764391hg38UCSC Ensembl
chr19:5658858..5764402hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38105545
hg19105545
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720841
Samples
Known GenesC19orf70, CATSPERD, HSD11B1L, LONP1, RPL36, SAFB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556725
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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