A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467801



Internal ID21125354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102444261..102444733hg38UCSC Ensembl
chr11:102314992..102315464hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196635
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467801
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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