A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6374951



Internal ID9014288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13926002..13930628hg38UCSC Ensembl
chr20:13906648..13911274hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg384627
hg194627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663578
Supporting Variants
SamplesHG00628
Known GenesSEL1L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6374951
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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