A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669851



Internal ID9589270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3504050..3507475hg38UCSC Ensembl
chr18:3504048..3507473hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383426
hg193426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv577e199
Supporting Variantsessv6352517
SamplesNA11994
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669851
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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