A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007746



Internal ID20574786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33140551..33144494hg38UCSC Ensembl
chr13:33714688..33718631hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg383944
hg193944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483252
Supporting Variants
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007746
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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