A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170061



Internal ID21314122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100975963..100980289hg38UCSC Ensembl
Outerchr8:100970966..100981353hg38UCSC Ensembl
Innerchr8:101988191..101992517hg19UCSC Ensembl
Outerchr8:101983194..101993581hg19UCSC Ensembl
Innerchr8:102057367..102061693hg18UCSC Ensembl
Outerchr8:102052370..102062757hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3810388
hg1910388
hg1810388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251479
SamplesMLY_8
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170061
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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