A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634942



Internal ID7021742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74400972..74402992hg38UCSC Ensembl
Innerchr14:74400993..74402971hg38UCSC Ensembl
Outerchr14:74400951..74403013hg38UCSC Ensembl
chr14:74867675..74869695hg19UCSC Ensembl
Innerchr14:74867696..74869674hg19UCSC Ensembl
Outerchr14:74867654..74869716hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382021
hg192021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15061245
SamplesHG03129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634942
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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