A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611869



Internal ID16399278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107492933..107496888hg38UCSC Ensembl
Innerchr8:108505161..108509116hg19UCSC Ensembl
Innerchr8:108574337..108578292hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg383956
hg193956
hg183956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12256n54
Supporting Variantsnssv1118303
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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