A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009382



Internal ID20576422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48593612..48593868hg38UCSC Ensembl
chr13:49167748..49168004hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00101


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