A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939038



Internal ID21359107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59442200..59442200hg38UCSC Ensembl
chr20:58017255..58017255hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188210
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939038
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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