A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610098



Internal ID16050821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7757106..8187522hg38UCSC Ensembl
Innerchr8:7614628..8045044hg19UCSC Ensembl
Innerchr8:7652038..8082454hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38430417
hg19430417
hg18430417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11928n54
Supporting Variantsnssv1105807
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4A, FAM66E, FAM90A10P, MIR548I3, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L3, USP17L8, ZNF705B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610098
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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