A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046429



Internal ID98753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70386791..70396980hg38UCSC Ensembl
chr11:70232897..70243086hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810190
hg1910190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500972
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046429
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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