A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007614



Internal ID18750145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3884069..4169596hg38UCSC Ensembl
Innerchr4:3885796..4171323hg19UCSC Ensembl
Innerchr4:3855594..4222224hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38285528
hg19285528
hg18366631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5084n100
Supporting Variantsnssv3616135
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)nsv1007614
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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