A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841442



Internal ID22616377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138302024..138307011hg38UCSC Ensembl
chr5:137637713..137642700hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg384988
hg194988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495547
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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