A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465106



Internal ID21122659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32710956..32719546hg38UCSC Ensembl
chr11:32732502..32741092hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388591
hg198591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989729
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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