A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634990



Internal ID7021790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76703264..76719081hg38UCSC Ensembl
Innerchr14:76703298..76719048hg38UCSC Ensembl
Outerchr14:76703231..76719115hg38UCSC Ensembl
chr14:77169607..77185424hg19UCSC Ensembl
Innerchr14:77169641..77185391hg19UCSC Ensembl
Outerchr14:77169574..77185458hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3815818
hg1915818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15068948, essv15068947
SamplesHG02678, HG03849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634990
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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