A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040571



Internal ID94755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1647920..1665773hg38UCSC Ensembl
chr11:1669150..1687003hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3817854
hg1917854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499337
Supporting Variants
Samples
Known GenesFAM99A, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040571
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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