A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029069



Internal ID18771601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96386..458905hg38UCSC Ensembl
Innerchr8:46386..408905hg19UCSC Ensembl
Innerchr8:36386..398905hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38362520
hg19362520
hg18362520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6789n100
Supporting Variantsnssv3674903, nssv3674904
Samples
Known GenesFAM87A, FBXO25, OR4F21, RPL23AP53, ZNF596
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029069
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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