A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045328



Internal ID97975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47294382..47345018hg38UCSC Ensembl
chr11:47315933..47366569hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3850637
hg1950637
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558041
Supporting Variants
Samples
Known GenesMADD, MYBPC3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045328
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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