A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561224



Internal ID334209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186622707..186667582hg38UCSC Ensembl
chr4:187543861..187588736hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3844876
hg1944876
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962327
Samples
Known GenesFAT1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561224
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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