A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466523



Internal ID21124076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118536436..118539401hg38UCSC Ensembl
chr11:118407151..118410116hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987195
Samples
Known GenesTMEM25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466523
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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