A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020496



Internal ID19109715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12383639..12418220hg38UCSC Ensembl
Innerchr8:12241148..12275729hg19UCSC Ensembl
Innerchr8:12285519..12320100hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3834582
hg1934582
hg1834582
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7046n100
Supporting Variantsnssv3664886, nssv3664887
Samples
Known GenesDEFB109P1, FAM66A, FAM90A25P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020496
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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