A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14340492



Internal ID22232888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32907037..32916231hg38UCSC Ensembl
chr8:32764555..32773749hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389195
hg199195
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223925
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14340492
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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