A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6465342



Internal ID9442745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113802582..113803662hg38UCSC Ensembl
chr13:114505555..114506635hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667518
Supporting Variants
SamplesNA20814
Known GenesTMEM255B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6465342
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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