A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv188n21



Internal ID20131909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54471593..54740381hg38UCSC Ensembl
chr18:51997963..52407612hg19UCSC Ensembl
chr18:50251961..50558610hg18UCSC Ensembl
chr18:50251961..50558610hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38268789
hg19409650
hg18306650
hg17306650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519491, nsv528776
Samples
Known GenesDYNAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv188n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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