A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv184n21



Internal ID20131905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3526777..5930980hg38UCSC Ensembl
chr18:3526775..5930979hg19UCSC Ensembl
chr18:3516775..5920979hg18UCSC Ensembl
chr18:3516775..5920979hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382404204
hg192404205
hg182404205
hg172404205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521876, nsv521255
Samples
Known GenesC18orf42, DLGAP1, DLGAP1-AS1, DLGAP1-AS3, DLGAP1-AS4, DLGAP1-AS5, EPB41L3, LINC00526, LINC00667, LOC645355, MIR3976, MIR6718, TMEM200C, ZBTB14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv184n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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