A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5464650



Internal ID9543920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140712153..140712449hg38UCSC Ensembl
chr4:141633307..141633603hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661875
Supporting Variants
SamplesNA19076
Known GenesTBC1D9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5464650
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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