A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458936



Internal ID21116489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78424252..78424584hg38UCSC Ensembl
chr11:78135298..78135630hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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