A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1118239



Internal ID15971425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106427810..106482690hg38UCSC Ensembl
Innerchr8:107440038..107494918hg19UCSC Ensembl
Innerchr8:107509214..107564094hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3854881
hg1954881
hg1854881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611844
Supporting Variants
Samples
Known GenesOXR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1118239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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