A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007135



Internal ID18749666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4165406hg38UCSC Ensembl
Innerchr4:3885796..4167133hg19UCSC Ensembl
Innerchr4:3855594..4218034hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38281338
hg19281338
hg18362441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5084n100
Supporting Variantsnssv3616134, nssv3616133
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)nsv1007135
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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