A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457706



Internal ID21115259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34670365..34670685hg38UCSC Ensembl
chr11:34691912..34692232hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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