A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006783



Internal ID20573823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105703437..105712908hg38UCSC Ensembl
chr13:106355786..106365257hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg389472
hg199472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494256
Supporting Variants
Samples
Known GenesLINC00343
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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