A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214637



Internal ID22361232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21871943..21872084hg38UCSC Ensembl
chr8:21729454..21729595hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340345, nssv14340344
SamplesHG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214637
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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