A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv152n21



Internal ID20131873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61837610..62047927hg38UCSC Ensembl
chr15:62129809..62340126hg19UCSC Ensembl
chr15:59917101..60127418hg18UCSC Ensembl
chr15:59917101..60127418hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38210318
hg19210318
hg18210318
hg17210318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516639, nsv527451
Samples
Known GenesVPS13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv152n21
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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