A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6311880



Internal ID9768988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26991656..26992377hg38UCSC Ensembl
chr18:24571620..24572341hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658895
Supporting Variants
SamplesNA19726
Known GenesCHST9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6311880
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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