A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892507



Internal ID19183327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39827571..39895440hg38UCSC Ensembl
Outerchr14:39827571..39895440hg38UCSC Ensembl
Innerchr14:40296775..40364644hg19UCSC Ensembl
Outerchr14:40296775..40364644hg19UCSC Ensembl
Innerchr14:39366526..39434395hg18UCSC Ensembl
Outerchr14:39366526..39434395hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3867870
hg1967870
hg1867870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796780
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892507
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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