A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236776



Internal ID20803816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12334934..13449871hg38UCSC Ensembl
chr9:12334934..13449870hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381114938
hg191114937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428413
Supporting Variants
Samples
Known GenesFLJ41200, LURAP1L, MPDZ, TYRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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