A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990691



Internal ID61209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169535002..169539535hg38UCSC Ensembl
chr6:169935098..169939631hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384534
hg194534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458549
Supporting Variants
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990691
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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