A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009122



Internal ID18751653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3855594..4170575hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg18314982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5084n100
Supporting Variantsnssv3616129, nssv3616128, nssv3616127
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009122
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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