A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475219



Internal ID21132772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132402777..132403403hg38UCSC Ensembl
chr11:132272671..132273297hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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