A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611855



Internal ID16399264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107492679..107493466hg38UCSC Ensembl
Innerchr8:108504907..108505694hg19UCSC Ensembl
Innerchr8:108574083..108574870hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12254n54
Supporting Variantsnssv1118253, nssv1118254
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611855
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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