A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589769



Internal ID16030492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14136822..14139133hg38UCSC Ensembl
Innerchr3:14178322..14180633hg19UCSC Ensembl
Innerchr3:14153323..14155634hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382312
hg192312
hg182312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959438
Samples
Known GenesTMEM43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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