A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944568



Internal ID21364637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45133446..45133446hg38UCSC Ensembl
chr3:45174938..45174938hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189238
SamplesHG002
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944568
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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