A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024685



Internal ID19113902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6717813..6765164hg38UCSC Ensembl
Innerchr8:6575334..6622685hg19UCSC Ensembl
Innerchr8:6562742..6610095hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847352
hg1947352
hg1847354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6877n100
Supporting Variantsnssv3677437
Samples
Known GenesAGPAT5, MIR4659A, MIR4659B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024685
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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