A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981648



Internal ID55122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42554768..42554878hg38UCSC Ensembl
chr6:42522506..42522616hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981648
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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