A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv187n21



Internal ID22766379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9177896..9178308hg38UCSC Ensembl
chr18:9177894..9178306hg19UCSC Ensembl
chr18:9167894..9168306hg18UCSC Ensembl
chr18:9167894..9168306hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38413
hg19413
hg18413
hg17413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516645, nsv526584
Samples
Known GenesANKRD12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv187n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer