A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006900



Internal ID20573940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105278230..105279478hg38UCSC Ensembl
chr13:105930581..105931829hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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