A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5690836



Internal ID8668239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105057308..105057452hg38UCSC Ensembl
chr14:105523645..105523789hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665589
Supporting Variants
SamplesHG00734
Known GenesGPR132
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5690836
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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