A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv164n21



Internal ID22766356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25938859..26009513hg38UCSC Ensembl
chr16:25950180..26020834hg19UCSC Ensembl
chr16:25857681..25928335hg18UCSC Ensembl
chr16:25857681..25928335hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3870655
hg1970655
hg1870655
hg1770655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523821, nsv524942
Samples
Known GenesHS3ST4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv164n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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