A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401902



Internal ID21059455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138278473..138288418hg38UCSC Ensembl
chr5:137614162..137624107hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg389946
hg199946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125330
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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