A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6591392



Internal ID8904797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28804809..28808183hg38UCSC Ensembl
chr14:29274015..29277389hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383375
hg193375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662085
Supporting Variants
SamplesHG00367
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6591392
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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