A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979106



Internal ID53449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12398554..12398558hg38UCSC Ensembl
chr6:12398786..12398790hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg385
hg195
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979106
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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