A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610095



Internal ID16397504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7551054..7578739hg38UCSC Ensembl
Innerchr8:7408576..7436261hg19UCSC Ensembl
Innerchr8:7395986..7423671hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3827686
hg1927686
hg1827686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11927n54
Supporting Variantsnssv1105804
Samples
Known GenesFAM90A7P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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