A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633897



Internal ID7020701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28002435..28051026hg38UCSC Ensembl
Innerchr14:28002435..28051026hg38UCSC Ensembl
Outerchr14:28001935..28051526hg38UCSC Ensembl
chr14:28471641..28520232hg19UCSC Ensembl
Innerchr14:28471641..28520232hg19UCSC Ensembl
Outerchr14:28471141..28520732hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3848592
hg1948592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv390e214
Supporting Variantsessv14949902, essv14949901, essv14949899, essv14949897, essv14949898, essv14949900
SamplesHG03960, HG03792, HG04001, HG02651, HG04099, HG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633897
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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