A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv395n21



Internal ID22766587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134233200..134236251hg38UCSC Ensembl
chr6:134554338..134557389hg19UCSC Ensembl
chr6:134596031..134599082hg18UCSC Ensembl
chr6:134596031..134599082hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383052
hg193052
hg183052
hg173052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523127, nsv521411
Samples
Known GenesSGK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv395n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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