A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373326



Internal ID22154791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68257829..68257889hg38UCSC Ensembl
chr15:68550167..68550227hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226501
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14373326
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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