A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv581e199



Internal ID22758354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9043662..9047489hg38UCSC Ensembl
chr18:9043660..9047487hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383828
hg193828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678858, esv2669185
SamplesNA20536
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv581e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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