A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110014



Internal ID15616514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37935047..38054626hg38UCSC Ensembl
Innerchr8:37792565..37912144hg19UCSC Ensembl
Innerchr8:37911723..38031301hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38119580
hg19119580
hg18119579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610947
Supporting Variants
Samples
Known GenesADRB3, EIF4EBP1, GOT1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1110014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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