A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051027



Internal ID101893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91933592..91934769hg38UCSC Ensembl
chr11:91666758..91667935hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051027
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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