A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047796



Internal ID99724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60275074..60281074hg38UCSC Ensembl
chr11:60042547..60048547hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498810
Supporting Variants
Samples
Known GenesMS4A4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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