A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610058



Internal ID16050781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7397983..7935485hg38UCSC Ensembl
Innerchr8:7255505..7793007hg19UCSC Ensembl
Innerchr8:7242915..7830417hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38537503
hg19537503
hg18587503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11911n54
Supporting Variantsnssv1105745, nssv1105746
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, DEFB4B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610058
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer