A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942693



Internal ID21362762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40998439..40998439hg38UCSC Ensembl
chr20:39627079..39627079hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188955
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942693
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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