A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5595071



Internal ID9810560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41002833..41016414hg38UCSC Ensembl
Outerchr14:41002796..41016464hg38UCSC Ensembl
Innerchr14:41472038..41485619hg19UCSC Ensembl
Outerchr14:41472001..41485669hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3813669
hg1913669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661917
Supporting Variants
SamplesNA19916
Known GenesLOC644919
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5595071
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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