A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv33e55



Internal ID22760983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66929809..67178536hg38UCSC Ensembl
chr10:68689567..68938294hg19UCSC Ensembl
chr10:68359573..68608300hg18UCSC Ensembl
chr10:68359573..68608300hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38248728
hg19248728
hg18248728
hg17248728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2750974, esv2750972, esv2750973
SamplesSPC_15, BEC_696, BEC_820
Known GenesCTNNA3, LRRTM3
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)dgv33e55
Frequency
Sample Size771
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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