A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169455



Internal ID21313938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8234503..8310952hg38UCSC Ensembl
Outerchr8:8229622..8313949hg38UCSC Ensembl
Innerchr8:8092025..8168474hg19UCSC Ensembl
Outerchr8:8087144..8171471hg19UCSC Ensembl
Innerchr8:8129435..8205884hg18UCSC Ensembl
Outerchr8:8124554..8208881hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3884328
hg1984328
hg1884328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252090
SamplesNGO_52
Known GenesFAM86B3P
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169455
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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