A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390091



Internal ID22270942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83176939..83176939hg38UCSC Ensembl
chr15:83845691..83845691hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560589
Supporting Variants
SamplesNA19239
Known GenesHDGFRP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390091
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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