A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457705



Internal ID21115258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46882270..46882640hg38UCSC Ensembl
chr11:46903821..46904191hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991117
Samples
Known GenesLRP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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