A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5810274



Internal ID8787677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3523609..3524675hg38UCSC Ensembl
chr18:3523607..3524673hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663925
Supporting Variants
SamplesNA18621
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5810274
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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