A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610037



Internal ID16050760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7338677..7598872hg38UCSC Ensembl
Innerchr8:7196199..7456394hg19UCSC Ensembl
Innerchr8:7183609..7443804hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38260196
hg19260196
hg18260196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11912n54
Supporting Variantsnssv1105709
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, FAM66B, FAM90A7P, PRR23D1, PRR23D2, SPAG11B, USP17L4, ZNF705G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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