A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610093



Internal ID16397502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7535252..7598872hg38UCSC Ensembl
Innerchr8:7392774..7456394hg19UCSC Ensembl
Innerchr8:7380184..7443804hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3863621
hg1963621
hg1863621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105802
Samples
Known GenesFAM90A7P, PRR23D1, PRR23D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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