A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466073



Internal ID21123626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98552023..98650521hg38UCSC Ensembl
chr11:98422753..98521251hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3898499
hg1998499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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