A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410006



Internal ID21067559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138321487..138332645hg38UCSC Ensembl
chr5:137657176..137668334hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3811159
hg1911159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125331
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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