A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466723



Internal ID21124276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130030118..130039267hg38UCSC Ensembl
chr11:129900013..129909162hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg389150
hg199150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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