A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5866367



Internal ID9879113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28595547..28605507hg38UCSC Ensembl
Outerchr14:28595499..28605557hg38UCSC Ensembl
Innerchr14:29064753..29074713hg19UCSC Ensembl
Outerchr14:29064705..29074763hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3810059
hg1910059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673801
Supporting Variants
SamplesNA20753
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5866367
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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