A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467384



Internal ID21124937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71280509..71283030hg38UCSC Ensembl
chr11:70991555..70994076hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382522
hg192522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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