A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031798



Internal ID18774332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7172456..7545521hg38UCSC Ensembl
Innerchr8:7029978..7403043hg19UCSC Ensembl
Innerchr8:7017388..7390453hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38373066
hg19373066
hg18373066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6898n100
Supporting Variantsnssv3677648
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4B, FAM66B, LINC00965, PRR23D1, PRR23D2, SPAG11B, USP17L1P, USP17L4, ZNF705G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031798
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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