A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561268



Internal ID334253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2409661..2423767hg38UCSC Ensembl
chr19:2409659..2423765hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3814107
hg1914107
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720391
Samples
Known GenesTMPRSS9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561268
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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