A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021914



Internal ID18764448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7396757..7535076hg38UCSC Ensembl
Innerchr8:7254279..7392598hg19UCSC Ensembl
Innerchr8:7241689..7380008hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38138320
hg19138320
hg18138320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6933n100
Supporting Variantsnssv3679606, nssv3679605
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021914
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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