A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052644



Internal ID102950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129318544..129318937hg38UCSC Ensembl
chr11:129188439..129188832hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562479
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052644
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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