A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527146



Internal ID22396531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76303628..76303745hg38UCSC Ensembl
chr8:77215863..77215980hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9223n152
Supporting Variantsnssv14343894, nssv14343897, nssv14343898, nssv14343892, nssv14343893, nssv14343896, nssv14343895, nssv14343899
SamplesHG00512, NA19238, NA19239, HG00731, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527146
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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