A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458400



Internal ID21115953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69246022..69247787hg38UCSC Ensembl
chr11:69013489..69015254hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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