A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611859



Internal ID16399268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107492679..107493758hg38UCSC Ensembl
Innerchr8:108504907..108505986hg19UCSC Ensembl
Innerchr8:108574083..108575162hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381080
hg191080
hg181080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12254n54
Supporting Variantsnssv1118262, nssv1118263, nssv1118261, nssv1118260, nssv1118264, nssv1118259
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611859
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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