A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv128e214



Internal ID20121551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50507424..50513989hg38UCSC Ensembl
chr10:52267184..52273749hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg386566
hg196566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3623206, esv3623208
SamplesNA21133, HG03931
Known GenesSGMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv128e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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