A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046797



Internal ID99011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65949607..65952126hg38UCSC Ensembl
chr11:65717078..65719597hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382520
hg192520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143577
Supporting Variants
Samples
Known GenesTSGA10IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046797
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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