A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938305



Internal ID21358374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27749220..27749220hg38UCSC Ensembl
chr2:27972087..27972087hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187824
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938305
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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