A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6313372



Internal ID9554386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65152398..65153596hg38UCSC Ensembl
chr14:65619116..65620314hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669140
Supporting Variants
SamplesNA19085
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6313372
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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