A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669281



Internal ID9935386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96582257..96585377hg38UCSC Ensembl
Outerchr14:96582209..96585431hg38UCSC Ensembl
Innerchr14:97048594..97051714hg19UCSC Ensembl
Outerchr14:97048546..97051768hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383223
hg193223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6573043
SamplesHG00156
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669281
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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