A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999899



Internal ID19159435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3912156..4112182hg38UCSC Ensembl
Innerchr4:3913883..4113909hg19UCSC Ensembl
Innerchr4:3964803..4164810hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38200027
hg19200027
hg18200008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5089n100
Supporting Variantsnssv3616157
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)nsv999899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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