A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032614



Internal ID19121836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:367480..411499hg38UCSC Ensembl
Innerchr8:317480..361499hg19UCSC Ensembl
Innerchr8:307480..351499hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3844020
hg1944020
hg1844020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674926
Samples
Known GenesFAM87A, FBXO25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032614
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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