A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468801



Internal ID21126354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32884301..32892300hg38UCSC Ensembl
chr11:32905847..32913846hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468801
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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