A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635545



Internal ID7022344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102171152..102173344hg38UCSC Ensembl
Innerchr14:102171160..102173337hg38UCSC Ensembl
Outerchr14:102171145..102173352hg38UCSC Ensembl
chr14:102637489..102639681hg19UCSC Ensembl
Innerchr14:102637497..102639674hg19UCSC Ensembl
Outerchr14:102637482..102639689hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109349, essv15109350, essv15109351, essv15109387, essv15109358, essv15109385, essv15109348, essv15109371, essv15109354, essv15109367, essv15109375, essv15109353, essv15109366, essv15109378, essv15109361, essv15109380, essv15109370, essv15109352, essv15109384, essv15109368, essv15109373, essv15109376, essv15109355, essv15109386, essv15109379, essv15109362, essv15109359, essv15109363, essv15109357, essv15109369, essv15109356, essv15109365, essv15109364, essv15109374, essv15109372, essv15109360, essv15109377, essv15109381, essv15109382, essv15109383
SamplesNA20761, NA11995, NA12414, HG01079, HG03015, NA12045, HG01486, HG00179, NA12812, NA20589, HG01351, NA19678, NA20795, NA20822, HG01628, HG01281, HG01767, HG01176, HG01525, NA19722, HG02439, NA20787, HG00275, NA20506, HG00239, HG01948, HG02604, HG01530, HG00258, HG02696, HG00278, HG02685, HG01108, NA20797, HG03703, HG01785, HG00112, NA20826, HG00274, HG02006
Known GenesWDR20
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635545
Frequency
Sample Size2504
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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