A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6570667



Internal ID9548070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75140320..75143049hg38UCSC Ensembl
Outerchr14:75140283..75143099hg38UCSC Ensembl
Innerchr14:75607023..75609752hg19UCSC Ensembl
Outerchr14:75606986..75609802hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382817
hg192817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673828
Supporting Variants
SamplesHG00662
Known GenesTMED10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6570667
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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