A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634502



Internal ID7021305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51272929..51279537hg38UCSC Ensembl
Innerchr14:51272941..51279526hg38UCSC Ensembl
Outerchr14:51272918..51279549hg38UCSC Ensembl
chr14:51739647..51746255hg19UCSC Ensembl
Innerchr14:51739659..51746244hg19UCSC Ensembl
Outerchr14:51739636..51746267hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg386609
hg196609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15009840
SamplesHG04222
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634502
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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