A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466363



Internal ID21123916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77654039..77655832hg38UCSC Ensembl
chr11:77365084..77366877hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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