A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027394



Internal ID18769926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7367834..7545918hg38UCSC Ensembl
Innerchr8:7225356..7403440hg19UCSC Ensembl
Innerchr8:7212766..7390850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38178085
hg19178085
hg18178085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6924n100
Supporting Variantsnssv3755003
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, PRR23D1, PRR23D2, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027394
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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