A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7548n54



Internal ID22775443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30377730..30417145hg38UCSC Ensembl
chr20:29612406..29651821hg19UCSC Ensembl
chr20:28226067..28265482hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3839416
hg1939416
hg1839416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585872, nsv585871, nsv585873
Samples
Known GenesFRG1B, MLLT10P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7548n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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