A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7437n54



Internal ID22775332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1914283..1915094hg38UCSC Ensembl
chr20:1894929..1895740hg19UCSC Ensembl
chr20:1842929..1843740hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38812
hg19812
hg18812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585256, nsv585257
Samples
Known GenesSIRPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7437n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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