A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385826



Internal ID22310011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83187222..83187318hg38UCSC Ensembl
chr15:83855974..83856070hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215148
Supporting Variants
SamplesNA19240
Known GenesHDGFRP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385826
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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