A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1012558



Internal ID15959828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166083189..166083600hg38UCSC Ensembl
Innerchr4:167004341..167004752hg19UCSC Ensembl
Innerchr4:167223791..167224202hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38412
hg19412
hg18412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596053
Supporting Variants
Samples
Known GenesTLL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1012558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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