A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986896



Internal ID58710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92498042..92498919hg38UCSC Ensembl
chr6:93207760..93208637hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986896
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001249


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