A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7902n54



Internal ID22775797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45448915..45484919hg38UCSC Ensembl
chr21:46868829..46904833hg19UCSC Ensembl
chr21:45693257..45729261hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3836005
hg1936005
hg1836005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587849, nsv587848
SamplesHGDP00433, HGDP00603
Known GenesCOL18A1, MIR6815
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7902n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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