A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029359



Internal ID19118578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12407033..12496209hg38UCSC Ensembl
Innerchr8:12264542..12353718hg19UCSC Ensembl
Innerchr8:12308913..12398089hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3889177
hg1989177
hg1889177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7069n100
Supporting Variantsnssv3666896
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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