A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988372



Internal ID59666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90771334..90775590hg38UCSC Ensembl
chr6:91481052..91485308hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384257
hg194257
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988372
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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