A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558413



Internal ID331478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31190134..31191079hg38UCSC Ensembl
chr5:31190241..31191186hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558413
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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