A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590701



Internal ID16378110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75431963..75863222hg38UCSC Ensembl
Innerchr3:75481114..75912373hg19UCSC Ensembl
Innerchr3:75563804..75995063hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38431260
hg19431260
hg18431260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8385n54
Supporting Variantsnssv965776
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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