A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563424



Internal ID336358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111815965..111872169hg38UCSC Ensembl
chr6:112137168..112193372hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3856205
hg1956205
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986753
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563424
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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