A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559176



Internal ID332218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133939544..133943810hg38UCSC Ensembl
chr5:133275235..133279501hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384267
hg194267
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559176
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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