A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938669



Internal ID21358738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3590500..3590500hg38UCSC Ensembl
chr2:3638090..3638090hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187801
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938669
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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