A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633771



Internal ID7020577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23013646..23015091hg38UCSC Ensembl
Innerchr14:23013647..23015090hg38UCSC Ensembl
Outerchr14:23013645..23015092hg38UCSC Ensembl
chr14:23482855..23484300hg19UCSC Ensembl
Innerchr14:23482856..23484299hg19UCSC Ensembl
Outerchr14:23482854..23484301hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14935059, essv14935060, essv14935061
SamplesHG02380, HG02373, HG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633771
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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