A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610154



Internal ID16397563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8244119..8470591hg38UCSC Ensembl
Innerchr8:8101641..8328101hg19UCSC Ensembl
Innerchr8:8139051..8365511hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38226473
hg19226461
hg18226461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105887
Samples
Known GenesFAM86B3P, SGK223
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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