A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227178



Internal ID22369755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102640589..102640661hg38UCSC Ensembl
chr8:103652817..103652889hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9280n152
Supporting Variantsnssv14342204, nssv14342205
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227178
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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