A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590690



Internal ID16378099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403949..75587298hg38UCSC Ensembl
Innerchr3:75453100..75636449hg19UCSC Ensembl
Innerchr3:75535790..75719139hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38183350
hg19183350
hg18183350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965756, nssv965758, nssv965757
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590690
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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