A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189864



Internal ID20756904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72025209..72302197hg38UCSC Ensembl
chr11:71736255..72013241hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38276989
hg19276987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470560
Supporting Variants
Samples
Known GenesANAPC15, CLPB, FOLR1, FOLR2, FOLR3, INPPL1, LAMTOR1, LRTOMT, MIR3165, NUMA1, PHOX2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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