A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022386



Internal ID19111604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12418220..12505127hg38UCSC Ensembl
Innerchr8:12275729..12362636hg19UCSC Ensembl
Innerchr8:12320100..12407007hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3886908
hg1986908
hg1886908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7069n100
Supporting Variantsnssv3666908
Samples
Known GenesFAM86B2, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022386
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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