A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015490



Internal ID19104707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123091015..123138750hg38UCSC Ensembl
Innerchr8:124103255..124150990hg19UCSC Ensembl
Innerchr8:124172436..124220171hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3847736
hg1947736
hg1847736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691498
Samples
Known GenesTBC1D31
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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