A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590675



Internal ID16378084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75400984..75554297hg38UCSC Ensembl
Innerchr3:75450135..75603448hg19UCSC Ensembl
Innerchr3:75532825..75686138hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38153314
hg19153314
hg18153314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965696
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590675
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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