A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017571



Internal ID19106788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7433385..7930428hg38UCSC Ensembl
Innerchr8:7290907..7787950hg19UCSC Ensembl
Innerchr8:7278317..7825360hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38497044
hg19497044
hg18547044
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6936n100
Supporting Variantsnssv3680213, nssv3756498, nssv3680208, nssv3680215, nssv3680212, nssv3680207, nssv3756499, nssv3680209, nssv3756508, nssv3756503, nssv3756500, nssv3756505, nssv3756506, nssv3756509, nssv3756511, nssv3680214, nssv3756510, nssv3756501, nssv3756497, nssv3756507, nssv3756502, nssv3680211, nssv3756504, nssv3680210
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017571
Frequency
Sample Size11257
Observed Gain8
Observed Loss16
Observed Complex0
Frequencyn/a


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