A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478494



Internal ID21136047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31864298..31864792hg38UCSC Ensembl
chr13:32438435..32438929hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008574
Samples
Known GenesEEF1DP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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