A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401896



Internal ID21059449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135928301..135935700hg38UCSC Ensembl
chr5:135263990..135271389hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214494
Samples
Known GenesFBXL21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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