A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189082



Internal ID20756122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112787717..112790625hg38UCSC Ensembl
chr13:113442031..113444939hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382909
hg192909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494553
Supporting Variants
Samples
Known GenesATP11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00011


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