A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635568



Internal ID7022367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102740863..102761967hg38UCSC Ensembl
Innerchr14:102741363..102761467hg38UCSC Ensembl
Outerchr14:102739863..102762967hg38UCSC Ensembl
chr14:103207200..103228304hg19UCSC Ensembl
Innerchr14:103207700..103227804hg19UCSC Ensembl
Outerchr14:103206200..103229304hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3821105
hg1921105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109988
SamplesHG01767
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635568
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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