A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610151



Internal ID16397560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8240557..8310891hg38UCSC Ensembl
Innerchr8:8098079..8168413hg19UCSC Ensembl
Innerchr8:8135489..8205823hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3870335
hg1970335
hg1870335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105884
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610151
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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