A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435814



Internal ID21093367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9272653..9282861hg38UCSC Ensembl
chr11:9294200..9304408hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810209
hg1910209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995418
Samples
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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