A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106254



Internal ID15959440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10558507..10603974hg38UCSC Ensembl
Innerchr8:10416017..10461484hg19UCSC Ensembl
Innerchr8:10453427..10498894hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3845468
hg1945468
hg1845468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610269
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106254
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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