A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047977



Internal ID99848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63672538..63677255hg38UCSC Ensembl
chr11:63440010..63444727hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384718
hg194718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507356
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047977
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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