A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553930



Internal ID327128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110239212..110259810hg38UCSC Ensembl
chr4:111160368..111180966hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3820599
hg1920599
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16955610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553930
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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