A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483755



Internal ID21141308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39977316..39977898hg38UCSC Ensembl
chr13:40551453..40552035hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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