A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4177n100



Internal ID22790264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226224617..226286635hg38UCSC Ensembl
chr2:227089333..227151351hg19UCSC Ensembl
chr2:226797577..226859595hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3862019
hg1962019
hg1862019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008856, nsv1000256
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4177n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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