A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1102104



Internal ID15955290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:380328..482146hg38UCSC Ensembl
Innerchr8:330328..432146hg19UCSC Ensembl
Innerchr8:320328..422146hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38101819
hg19101819
hg18101819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609454
Supporting Variants
Samples
Known GenesFAM87A, FBXO25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1102104
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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