A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792849



Internal ID19171499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94096847..94118727hg38UCSC Ensembl
Innerchr14:94563193..94585064hg19UCSC Ensembl
Innerchr14:93632946..93654817hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3821881
hg1921872
hg1821872
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892577
Supporting Variants
Samples
Known GenesIFI27, IFI27L1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792849
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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