A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14389858



Internal ID22211066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51953585..51954008hg38UCSC Ensembl
chr15:52245782..52246205hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218859
Supporting Variants
SamplesHG00732
Known GenesLEO1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14389858
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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