A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385623



Internal ID22268393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68286870..68286870hg38UCSC Ensembl
chr15:68579208..68579208hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560720
Supporting Variants
SamplesNA19238
Known GenesFEM1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385623
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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