A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463731



Internal ID21121284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38631535..38633812hg38UCSC Ensembl
chr11:38653085..38655362hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382278
hg192278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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