A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009225



Internal ID20576267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47458843..47459331hg38UCSC Ensembl
chr13:48032978..48033466hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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