A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988869



Internal ID60006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119794361..119795926hg38UCSC Ensembl
chr6:120115507..120117072hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988869
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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