A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029391



Internal ID18771922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7425444..7535076hg38UCSC Ensembl
Innerchr8:7282966..7392598hg19UCSC Ensembl
Innerchr8:7270376..7380008hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38109633
hg19109633
hg18109633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6933n100
Supporting Variantsnssv3680150
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029391
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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