A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610039



Internal ID16050762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7339419..7925394hg38UCSC Ensembl
Innerchr8:7196941..7782916hg19UCSC Ensembl
Innerchr8:7184351..7820326hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38585976
hg19585976
hg18635976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11913n54
Supporting Variantsnssv1105712
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, DEFB4B, FAM66B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610039
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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