A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990187



Internal ID60858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160828904..160843329hg38UCSC Ensembl
chr6:161249936..161264361hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3814426
hg1914426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468258
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990187
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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