A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv216e55



Internal ID22761166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104885045..105139752hg38UCSC Ensembl
chr6:105332920..105587627hg19UCSC Ensembl
chr6:105439613..105694320hg18UCSC Ensembl
chr6:105439613..105694320hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38254708
hg19254708
hg18254708
hg17254708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34996, esv34842
SamplesNA11881, NA10859
Known GenesBVES, BVES-AS1, LIN28B, LINC00577
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)dgv216e55
Frequency
Sample Size771
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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