A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401367



Internal ID21058920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128063701..128083600hg38UCSC Ensembl
chr5:127399393..127419292hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3819900
hg1919900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215407
Samples
Known GenesFLJ33630
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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