A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454180



Internal ID21111733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9300704..9312622hg38UCSC Ensembl
chr11:9322251..9334169hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811919
hg1911919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996434
Samples
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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