A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612141



Internal ID16052864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123883569..123994250hg38UCSC Ensembl
Innerchr8:124895809..125006490hg19UCSC Ensembl
Innerchr8:124964990..125075671hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38110682
hg19110682
hg18110682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12305n54
Supporting Variantsnssv1120521
Samples
Known GenesFER1L6, FER1L6-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612141
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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