A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559055



Internal ID332101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161124859..161135847hg38UCSC Ensembl
chr1:161094649..161105637hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3810989
hg1910989
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892364
Samples
Known GenesDEDD, NIT1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559055
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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