A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028579



Internal ID19117797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:130897626..131484902hg38UCSC Ensembl
Innerchr8:131909872..132497149hg19UCSC Ensembl
Innerchr8:131979054..132566331hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38587277
hg19587278
hg18587278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757371
Samples
Known GenesADCY8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028579
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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