A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554892



Internal ID328063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:22423799..22878784hg38UCSC Ensembl
chr5:22423908..22878893hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38454986
hg19454986
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963038
Samples
Known GenesCDH12
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554892
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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