A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556237



Internal ID329378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142014763..142060495hg38UCSC Ensembl
chr5:141394328..141440060hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3845733
hg1945733
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556237
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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