A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032739



Internal ID18775273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11786294..11858964hg38UCSC Ensembl
Innerchr8:11643803..11716473hg19UCSC Ensembl
Innerchr8:11681212..11753882hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3872671
hg1972671
hg1872671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3754240
Samples
Known GenesCTSB, FDFT1, NEIL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032739
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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