A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635328



Internal ID7022127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91753704..91761307hg38UCSC Ensembl
Innerchr14:91753712..91761300hg38UCSC Ensembl
Outerchr14:91753697..91761315hg38UCSC Ensembl
chr14:92220048..92227651hg19UCSC Ensembl
Innerchr14:92220056..92227644hg19UCSC Ensembl
Outerchr14:92220041..92227659hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg387604
hg197604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15097030
SamplesHG03057
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635328
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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