A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338680



Internal ID22282682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32265161..32268458hg38UCSC Ensembl
chr10:32554089..32557386hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210546
Supporting Variants
SamplesNA19239
Known GenesEPC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338680
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer