A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563121



Internal ID336058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182970432..182970531hg38UCSC Ensembl
chr4:183891585..183891684hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563121
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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