A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634060



Internal ID7020864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35426870..35429253hg38UCSC Ensembl
Innerchr14:35426893..35429230hg38UCSC Ensembl
Outerchr14:35426847..35429276hg38UCSC Ensembl
chr14:35896076..35898459hg19UCSC Ensembl
Innerchr14:35896099..35898436hg19UCSC Ensembl
Outerchr14:35896053..35898482hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382384
hg192384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14967710, essv14967711, essv14967712
SamplesNA19920, NA19171, HG03118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634060
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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