A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv984192



Internal ID16278148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192671511..192674109hg38UCSC Ensembl
Innerchr3:192389300..192391898hg19UCSC Ensembl
Innerchr3:193871994..193874592hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592884
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)nssv984192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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