A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024774



Internal ID19113991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12374760..12562661hg38UCSC Ensembl
Innerchr8:12232269..12420170hg19UCSC Ensembl
Innerchr8:12276640..12464541hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38187902
hg19187902
hg18187902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7054n100
Supporting Variantsnssv3682686, nssv3682685
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)nsv1024774
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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