A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939392



Internal ID21359461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39399389..39399389hg38UCSC Ensembl
chr15:39691590..39691590hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194583
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939392
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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