A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691502



Internal ID18989783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124048291..124194204hg38UCSC Ensembl
Innerchr8:125060532..125206445hg19UCSC Ensembl
Innerchr8:125129713..125275626hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38145914
hg19145914
hg18145914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023183
Supporting Variants
Samples
Known GenesFER1L6, FER1L6-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691502
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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