A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892505



Internal ID19183325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39664617..39692036hg38UCSC Ensembl
Outerchr14:39664617..39692036hg38UCSC Ensembl
Innerchr14:40133821..40161240hg19UCSC Ensembl
Outerchr14:40133821..40161240hg19UCSC Ensembl
Innerchr14:39203572..39230991hg18UCSC Ensembl
Outerchr14:39203572..39230991hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3827420
hg1927420
hg1827420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799675
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892505
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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