A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472062



Internal ID21129615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132712514..132713668hg38UCSC Ensembl
chr11:132582409..132583563hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988052
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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