A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471890



Internal ID21129443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70395660..70397066hg38UCSC Ensembl
chr11:70241766..70243172hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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