A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590668



Internal ID16378077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75397370..75568509hg38UCSC Ensembl
Innerchr3:75446521..75617660hg19UCSC Ensembl
Innerchr3:75529211..75700350hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38171140
hg19171140
hg18171140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965679
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590668
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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