A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051760



Internal ID102353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134036997..134037047hg38UCSC Ensembl
chr11:133906892..133906942hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534383
Supporting Variants
Samples
Known GenesLOC100128239
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051760
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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