A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986185



Internal ID58214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:67954647..67957190hg38UCSC Ensembl
chr6:68664539..68667082hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382544
hg192544
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986185
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003746


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