A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474831



Internal ID21132384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123834026..123844093hg38UCSC Ensembl
chr11:123704734..123714801hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3810068
hg1910068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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