A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590412



Internal ID16377821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61138584..61142394hg38UCSC Ensembl
Innerchr3:61124257..61128067hg19UCSC Ensembl
Innerchr3:61099297..61103107hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg383811
hg193811
hg183811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8345n54
Supporting Variantsnssv963415
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590412
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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