A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843467



Internal ID22618402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69295938..69301702hg38UCSC Ensembl
chr5:68591765..68597529hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg385765
hg195765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499921
Samples
Known GenesCCDC125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843467
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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