A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455930



Internal ID21113483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117824778..117826942hg38UCSC Ensembl
chr11:117695493..117697657hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194972
Samples
Known GenesFXYD2, FXYD6-FXYD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455930
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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