A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017140



Internal ID19106357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12620173hg38UCSC Ensembl
Innerchr8:12260915..12477682hg19UCSC Ensembl
Innerchr8:12305286..12522053hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38216768
hg19216768
hg18216768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7056n100
Supporting Variantsnssv3666870
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017140
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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