A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6449666



Internal ID9427069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42672718..42677772hg38UCSC Ensembl
chr18:40252683..40257737hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg385055
hg195055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660678
Supporting Variants
SamplesNA19920
Known GenesLINC00907
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6449666
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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