A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465013



Internal ID21122566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115318101..115416700hg38UCSC Ensembl
chr11:115188820..115287418hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3898600
hg1998599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986988
Samples
Known GenesCADM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465013
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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