A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943586



Internal ID21363655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66864649..66864649hg38UCSC Ensembl
chr15:67156987..67156987hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195007
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943586
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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