A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979894



Internal ID53973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3884960..3887231hg38UCSC Ensembl
chr6:3885194..3887465hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382272
hg192272
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979894
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.025913


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