A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634939



Internal ID7021739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74365149..74366714hg38UCSC Ensembl
Innerchr14:74365149..74366714hg38UCSC Ensembl
Outerchr14:74364830..74367002hg38UCSC Ensembl
chr14:74831852..74833417hg19UCSC Ensembl
Innerchr14:74831852..74833417hg19UCSC Ensembl
Outerchr14:74831533..74833705hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15061233, essv15061231, essv15061230, essv15061232, essv15061235, essv15061234, essv15061237, essv15061236, essv15061238
SamplesNA19399, HG02624, NA19451, HG02439, HG03132, NA19031, NA19390, NA18505, HG03303
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634939
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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