A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634862



Internal ID7021662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70429461..70433353hg38UCSC Ensembl
Innerchr14:70429478..70433336hg38UCSC Ensembl
Outerchr14:70429444..70433370hg38UCSC Ensembl
chr14:70896178..70900070hg19UCSC Ensembl
Innerchr14:70896195..70900053hg19UCSC Ensembl
Outerchr14:70896161..70900087hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383893
hg193893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15052686
SamplesNA18643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634862
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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