A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555921



Internal ID329070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51232913..51232919hg38UCSC Ensembl
chr19:51736168..51736174hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg387
hg197
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725375
Samples
Known GenesCD33
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555921
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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