A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635387



Internal ID7022186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94679795..94683592hg38UCSC Ensembl
Innerchr14:94679813..94683574hg38UCSC Ensembl
Outerchr14:94679777..94683610hg38UCSC Ensembl
chr14:95146132..95149929hg19UCSC Ensembl
Innerchr14:95146150..95149911hg19UCSC Ensembl
Outerchr14:95146114..95149947hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383798
hg193798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103232
SamplesHG04099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635387
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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