A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563903



Internal ID336829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172455536..172456236hg38UCSC Ensembl
chr3:172173326..172174026hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563903
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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