A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020808



Internal ID21930151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33618454..33619184hg38UCSC Ensembl
chr13:34192591..34193321hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614563
Samples
Known GenesSTARD13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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