A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485677



Internal ID21143230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26655674..26656268hg38UCSC Ensembl
chr13:27229811..27230405hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007479
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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