A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002732



Internal ID18745264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3899113..4182551hg38UCSC Ensembl
Innerchr4:3900840..4184278hg19UCSC Ensembl
Innerchr4:3870638..4235179hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38283439
hg19283439
hg18364542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5084n100
Supporting Variantsnssv3616146
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)nsv1002732
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer