A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470944



Internal ID21128497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119533919..119550440hg38UCSC Ensembl
chr11:119404629..119421151hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3816522
hg1916523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470944
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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