A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674101



Internal ID9940206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26053317..26053677hg38UCSC Ensembl
chr18:23633281..23633641hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5855710, essv6549982, essv6279447, essv5626071, essv6482819
SamplesNA18502, NA18510, NA18907, NA19108, HG01342
Known GenesSS18
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674101
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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