A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106984



Internal ID15613484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092262..16208972hg38UCSC Ensembl
Innerchr8:15949771..16066481hg19UCSC Ensembl
Innerchr8:15994142..16110852hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38116711
hg19116711
hg18116711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610590
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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