A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv99n21



Internal ID20131820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106959817..106974102hg38UCSC Ensembl
chr12:107353595..107367880hg19UCSC Ensembl
chr12:105877725..105892010hg18UCSC Ensembl
chr12:105856062..105870347hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3814286
hg1914286
hg1814286
hg1714286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524439, nsv525081
Samples
Known GenesC12orf23
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv99n21
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