A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459335



Internal ID21116888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34681507..34682298hg38UCSC Ensembl
chr11:34703054..34703845hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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