A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040318



Internal ID94583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9350376..9362131hg38UCSC Ensembl
chr11:9371923..9383678hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811756
hg1911756
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556606
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040318
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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