A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590688



Internal ID16378097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403949..75555318hg38UCSC Ensembl
Innerchr3:75453100..75604469hg19UCSC Ensembl
Innerchr3:75535790..75687159hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38151370
hg19151370
hg18151370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965753, nssv965752
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590688
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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