A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465275



Internal ID21122828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112536731..112544742hg38UCSC Ensembl
chr11:112407454..112415465hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg388012
hg198012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986807
Samples
Known GenesLOC387810
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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