A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223925



Internal ID22367537
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340492, nssv14340491, nssv14340487, nssv14340493, nssv14340489, nssv14340488, nssv14340494, nssv14340490, nssv14340495
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223925
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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