A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471618



Internal ID21129171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41722861..41723280hg38UCSC Ensembl
chr11:41744411..41744830hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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