A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457525



Internal ID21115078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33241222..33243747hg38UCSC Ensembl
chr11:33262768..33265293hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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