A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021694



Internal ID18764228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7465919..7930334hg38UCSC Ensembl
Innerchr8:7323441..7787856hg19UCSC Ensembl
Innerchr8:7310851..7825266hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38464416
hg19464416
hg18514416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6911n100
Supporting Variantsnssv3753602
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)nsv1021694
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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