A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892499



Internal ID18836633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34900273..35107577hg38UCSC Ensembl
Outerchr14:34900273..35107577hg38UCSC Ensembl
Innerchr14:35369479..35576783hg19UCSC Ensembl
Outerchr14:35369479..35576783hg19UCSC Ensembl
Innerchr14:34439230..34646534hg18UCSC Ensembl
Outerchr14:34439230..34646534hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38207305
hg19207305
hg18207305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783924
Samples
Known GenesFAM177A1, IGBP1P1, PPP2R3C, SRP54
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892499
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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