A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv960n54



Internal ID22768855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13527805..13529347hg38UCSC Ensembl
chr10:13569805..13571347hg19UCSC Ensembl
chr10:13609811..13611353hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381543
hg191543
hg181543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549993, nsv549992, nsv549994, nsv549995, nsv549990
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv960n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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