A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987992



Internal ID59424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110728037..110822467hg38UCSC Ensembl
chr6:111049240..111143670hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3894431
hg1994431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469677
Supporting Variants
Samples
Known GenesAMD1, CDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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