A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456943



Internal ID21114496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80009379..80009760hg38UCSC Ensembl
chr11:79720422..79720803hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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