A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450014



Internal ID21107567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13514084..13523308hg38UCSC Ensembl
chr11:13535631..13544855hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg389225
hg199225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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