A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927858



Internal ID21347928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50198107..50198107hg38UCSC Ensembl
chr20:48814644..48814644hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188195
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927858
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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