A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015569



Internal ID19104786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7433385..7952372hg38UCSC Ensembl
Innerchr8:7290907..7809894hg19UCSC Ensembl
Innerchr8:7278317..7847304hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38518988
hg19518988
hg18568988
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6936n100
Supporting Variantsnssv3680237, nssv3756517, nssv3756519, nssv3680241, nssv3680242, nssv3680238, nssv3680236, nssv3680234, nssv3756515, nssv3680231, nssv3680239, nssv3680233, nssv3756518, nssv3756513, nssv3680240, nssv3756514, nssv3680235, nssv3680232, nssv3756516
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)nsv1015569
Frequency
Sample Size11257
Observed Gain10
Observed Loss9
Observed Complex0
Frequencyn/a


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