A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007519



Internal ID20574559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27900473..27913513hg38UCSC Ensembl
chr13:28474610..28487650hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3813041
hg1913041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490010
Supporting Variants
Samples
Known GenesPDX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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