A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1319n54



Internal ID22769214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86366299..86367707hg38UCSC Ensembl
chr10:88126056..88127464hg19UCSC Ensembl
chr10:88116036..88117444hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381409
hg191409
hg181409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551781, nsv551780, nsv551779
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1319n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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