A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462780



Internal ID21120333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62563058..62565021hg38UCSC Ensembl
chr11:62330530..62332493hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381964
hg191964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993214
Samples
Known GenesEEF1G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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