A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025759



Internal ID18768291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21908590..21974708hg38UCSC Ensembl
Innerchr8:21766101..21832219hg19UCSC Ensembl
Innerchr8:21822047..21888165hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3866119
hg1966119
hg1866119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7131n100
Supporting Variantsnssv3685344, nssv3685345
Samples
Known GenesDOK2, XPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025759
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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