A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677940



Internal ID9944045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58064088..58064208hg38UCSC Ensembl
Outerchr14:58064051..58064258hg38UCSC Ensembl
Innerchr14:58530806..58530926hg19UCSC Ensembl
Outerchr14:58530769..58530976hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6101743, essv6513359, essv6000454, essv5847844
SamplesNA19379, NA19382, NA19404, NA19428
Known GenesC14orf37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677940
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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