A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635284



Internal ID7022083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88879010..88892598hg38UCSC Ensembl
Innerchr14:88879012..88892596hg38UCSC Ensembl
Outerchr14:88879008..88892600hg38UCSC Ensembl
chr14:89345354..89358942hg19UCSC Ensembl
Innerchr14:89345356..89358940hg19UCSC Ensembl
Outerchr14:89345352..89358944hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3813589
hg1913589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15092904, essv15092905, essv15092903
SamplesHG02102, HG01241, NA18501
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635284
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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