A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170010



Internal ID21314071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119298868..119305986hg38UCSC Ensembl
Outerchr8:119284309..119312668hg38UCSC Ensembl
Innerchr8:120311108..120318226hg19UCSC Ensembl
Outerchr8:120296549..120324908hg19UCSC Ensembl
Innerchr8:120380289..120387407hg18UCSC Ensembl
Outerchr8:120365730..120394089hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3828360
hg1928360
hg1828360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249181
SamplesMLY_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170010
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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