A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015574



Internal ID18758108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7357077..7918809hg38UCSC Ensembl
Innerchr8:7214599..7776331hg19UCSC Ensembl
Innerchr8:7202009..7813741hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38561733
hg19561733
hg18611733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6909n100
Supporting Variantsnssv3754163, nssv3754162
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, DEFB4B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015574
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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