A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459146



Internal ID21116699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105093408..105151127hg38UCSC Ensembl
chr11:104964135..105021854hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3857720
hg1957720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985681
Samples
Known GenesCARD17, CARD18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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