A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409088



Internal ID21066641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106500095..108059309hg38UCSC Ensembl
chr5:105835796..107395010hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381559215
hg191559215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212704
Samples
Known GenesEFNA5, FBXL17, LOC102467213
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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