A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590649



Internal ID16378058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75370585..75523048hg38UCSC Ensembl
Innerchr3:75419736..75572199hg19UCSC Ensembl
Innerchr3:75502426..75654889hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38152464
hg19152464
hg18152464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8380n54
Supporting Variantsnssv965636
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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