A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635569



Internal ID7022368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102761494..102763570hg38UCSC Ensembl
Innerchr14:102761511..102763553hg38UCSC Ensembl
Outerchr14:102761477..102763587hg38UCSC Ensembl
chr14:103227831..103229907hg19UCSC Ensembl
Innerchr14:103227848..103229890hg19UCSC Ensembl
Outerchr14:103227814..103229924hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109989
SamplesHG02082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635569
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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