A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7037n54



Internal ID22774932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:123521892..123578836hg38UCSC Ensembl
chr2:124279468..124336412hg19UCSC Ensembl
chr2:123995938..124052882hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3856945
hg1956945
hg1856945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582879, nsv582881, nsv582882
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7037n54
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