A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050272



Internal ID101415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112292849..112297885hg38UCSC Ensembl
chr11:112163572..112168608hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050272
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001249


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