A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635250



Internal ID7022049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87137837..87165053hg38UCSC Ensembl
Innerchr14:87138337..87164553hg38UCSC Ensembl
Outerchr14:87136837..87166053hg38UCSC Ensembl
chr14:87604181..87631397hg19UCSC Ensembl
Innerchr14:87604681..87630897hg19UCSC Ensembl
Outerchr14:87603181..87632397hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3827217
hg1927217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv415e214
Supporting Variantsessv15092058
SamplesHG02879
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635250
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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