A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459857



Internal ID21117410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108347901..108348800hg38UCSC Ensembl
chr11:108218628..108219527hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986353
Samples
Known GenesATM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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