A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1120524



Internal ID15973710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124045487..124194262hg38UCSC Ensembl
Innerchr8:125057728..125206503hg19UCSC Ensembl
Innerchr8:125126909..125275684hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38148776
hg19148776
hg18148776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612144
Supporting Variants
Samples
Known GenesFER1L6, FER1L6-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1120524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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