A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677104



Internal ID9943209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10160727..10160977hg38UCSC Ensembl
chr18:10160724..10160974hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5591423, essv6181263, essv6387296, essv6556282, essv6421182, essv6480370, essv5989654, essv6314380
SamplesNA19397, NA19381, NA19379, NA19382, NA19404, NA19385, NA19099, NA19834
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677104
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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