A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009259



Internal ID20576301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47866907..47867949hg38UCSC Ensembl
chr13:48441042..48442084hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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