A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14340324



Internal ID22264861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21352535..21352802hg38UCSC Ensembl
chr8:21210046..21210313hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528599
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14340324
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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