A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1118302



Internal ID15971488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107492933..107493957hg38UCSC Ensembl
Innerchr8:108505161..108506185hg19UCSC Ensembl
Innerchr8:108574337..108575361hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381025
hg191025
hg181025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611868
Supporting Variants
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1118302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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