A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv186n21



Internal ID22766378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8563624..8582181hg38UCSC Ensembl
chr18:8563622..8582179hg19UCSC Ensembl
chr18:8553622..8572179hg18UCSC Ensembl
chr18:8553622..8572179hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3818558
hg1918558
hg1818558
hg1718558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519772, nsv524077
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv186n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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