A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556163



Internal ID329307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18084798..18086372hg38UCSC Ensembl
chr5:18084907..18086481hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556163
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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