A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561127



Internal ID334114
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 StatusM
Merged Variants
Supporting Variantsnssv16904388
Samples
Known GenesST6GALNAC3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561127
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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