A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026077



Internal ID19115294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12374760..12649550hg38UCSC Ensembl
Innerchr8:12232269..12507059hg19UCSC Ensembl
Innerchr8:12276640..12551430hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38274791
hg19274791
hg18274791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7056n100
Supporting Variantsnssv3663535, nssv3755698, nssv3663536, nssv3755699, nssv3663534, nssv3755696, nssv3755697
Samples
Known GenesDEFB109P1, FAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC649352, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026077
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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