A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043994



Internal ID97063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43080272..43083440hg38UCSC Ensembl
chr11:43101822..43104990hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg383169
hg193169
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043994
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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