A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051588



Internal ID102241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127776364..127782700hg38UCSC Ensembl
chr11:127646259..127652595hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg386337
hg196337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051588
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009328


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