A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901401



Internal ID22676551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45096788..45098384hg38UCSC Ensembl
chr3:45138280..45139876hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381597
hg191597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427878
Samples
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901401
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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