A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982876



Internal ID55946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56042851..56047991hg38UCSC Ensembl
chr6:55907649..55912789hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg385141
hg195141
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982876
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.027318


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