A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv984198



Internal ID16278154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192671703..192674071hg38UCSC Ensembl
Innerchr3:192389492..192391860hg19UCSC Ensembl
Innerchr3:193872186..193874554hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382369
hg192369
hg182369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592887
Supporting Variants
Samples
Known GenesFGF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv984198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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