A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049654



Internal ID100996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86327738..86327941hg38UCSC Ensembl
chr11:86038780..86038983hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507528
Supporting Variants
Samples
Known GenesC11orf73
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049654
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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