A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381709



Internal ID22195532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57480248..57480248hg38UCSC Ensembl
chr15:57772446..57772446hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560463
Supporting Variants
SamplesHG00731
Known GenesCGNL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381709
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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