A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034444



Internal ID19123666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25117973..25152127hg38UCSC Ensembl
Innerchr8:24975488..25009642hg19UCSC Ensembl
Innerchr8:25031405..25065559hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3834155
hg1934155
hg1834155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7145n100
Supporting Variantsnssv3685477
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034444
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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