A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475279



Internal ID21132832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132736683..132737313hg38UCSC Ensembl
chr11:132606578..132607208hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988055
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475279
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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