A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559264



Internal ID332302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157186242..157204025hg38UCSC Ensembl
chr4:158107394..158125177hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3817784
hg1917784
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559264
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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