A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470939



Internal ID21128492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112174947..112213940hg38UCSC Ensembl
chr11:112045670..112084663hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3838994
hg1938994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986788
Samples
Known GenesBCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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