A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351749



Internal ID22207859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67784938..67795565hg38UCSC Ensembl
chr10:69544696..69555323hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810628
hg1910628
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223381
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351749
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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