A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv292n21



Internal ID22766484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97037479..97135275hg38UCSC Ensembl
chr3:96756323..96854119hg19UCSC Ensembl
chr3:98239013..98336809hg18UCSC Ensembl
chr3:98239013..98336809hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3897797
hg1997797
hg1897797
hg1797797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522959, nsv525805
Samples
Known GenesEPHA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv292n21
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