A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904388



Internal ID3746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76453502..76479106hg38UCSC Ensembl
chr1:76919187..76944791hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3825605
hg1925605
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561127
Supporting Variants
Samples
Known GenesST6GALNAC3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904388
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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