A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv211e55



Internal ID20126690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29868686..29948476hg38UCSC Ensembl
chr6:29836463..29916253hg19UCSC Ensembl
chr6:29944442..30024232hg18UCSC Ensembl
chr6:29944442..30024232hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3879791
hg1979791
hg1879791
hg1779791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752113, esv34987, esv34603
SamplesNA18951, BEC_104, NA12760
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv211e55
Frequency
Sample Size771
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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