A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969862



Internal ID47223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135519327..135721578hg38UCSC Ensembl
chr6:135840465..136042716hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38202252
hg19202252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471143
Supporting Variants
Samples
Known GenesLINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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