A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893675



Internal ID22668739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138302249..138307095hg38UCSC Ensembl
chr5:137637938..137642784hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg384847
hg194847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418911
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893675
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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