A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462095



Internal ID21119648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132908867..132909390hg38UCSC Ensembl
chr11:132778762..132779285hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988074
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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