A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485430



Internal ID21142983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22218667..22219076hg38UCSC Ensembl
chr13:22792806..22793215hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008046
Samples
Known GenesLINC00540
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485430
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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