A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658133



Internal ID9924238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:88122941..88123808hg38UCSC Ensembl
Outerchr14:88122904..88123858hg38UCSC Ensembl
Innerchr14:88589285..88590152hg19UCSC Ensembl
Outerchr14:88589248..88590202hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5951244
SamplesHG00119
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658133
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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