A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14342821



Internal ID22210509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95080400..95080489hg38UCSC Ensembl
chr8:96092628..96092717hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213250
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14342821
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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