A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907356



Internal ID5690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5237993..5268583hg38UCSC Ensembl
chr1:5298053..5328643hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3830591
hg1930591
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564098
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907356
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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