A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026037



Internal ID18768569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25414848..25473361hg38UCSC Ensembl
Innerchr8:25272364..25330877hg19UCSC Ensembl
Innerchr8:25328281..25386794hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3858514
hg1958514
hg1858514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7148n100
Supporting Variantsnssv3685500
Samples
Known GenesCDCA2, GNRH1, KCTD9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026037
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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