A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469538



Internal ID21127091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35617801..35621700hg38UCSC Ensembl
chr11:35639349..35643248hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191847
Samples
Known GenesFJX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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