A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611863



Internal ID16399272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107492733..107493572hg38UCSC Ensembl
Innerchr8:108504961..108505800hg19UCSC Ensembl
Innerchr8:108574137..108574976hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12254n54
Supporting Variantsnssv1118295, nssv1118296
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611863
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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