A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027079



Internal ID19116298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27902814..28001752hg38UCSC Ensembl
Innerchr8:27760331..27859269hg19UCSC Ensembl
Innerchr8:27816250..27915188hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3898939
hg1998939
hg1898939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7155n100
Supporting Variantsnssv3685528
Samples
Known GenesSCARA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027079
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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