A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672373



Internal ID9591792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102877121..102877502hg38UCSC Ensembl
Outerchr14:102876944..102877684hg38UCSC Ensembl
Innerchr14:103343458..103343839hg19UCSC Ensembl
Outerchr14:103343281..103344021hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5666952, essv5989464, essv5430557, essv6500608, essv6457772, essv5713509, essv5784123, essv6578768, essv5587789, essv5983282, essv5447877, essv6370708, essv5788900, essv6063865, essv5507800, essv6494424, essv6351173, essv5950889, essv5861954, essv5979621, essv6372494, essv5403865, essv6588863, essv5904306, essv6249754
SamplesNA19819, NA19404, NA19437, NA19311, NA19223, NA19359, NA19834, NA19147, NA19428, NA19982, NA20356, HG00259, NA19256, NA19313, NA19129, NA20126, NA18502, NA18910, NA19394, NA20289, NA20287, HG01108, NA18908, NA19448, NA19439
Known GenesTRAF3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672373
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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