A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv91e55



Internal ID22761041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19961833..20994922hg38UCSC Ensembl
chr15:20167086..21200251hg19UCSC Ensembl
chr15:18427100..19464910hg18UCSC Ensembl
chr15:18427100..19464910hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381033090
hg191033166
hg181037811
hg171037811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2751293, esv2751297, esv2751366, esv35163, esv2751292, esv2751364, esv2751295, esv2751365, esv2751296, esv2751464, esv2751294, esv2751369
SamplesBEC_337, BEC_687, BEC_701, BEC_584, NA19194, BEC_411, BEC_40, SPC_184, BEC_730, NA11882, BEC_343, SPC_128
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
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)dgv91e55
Frequency
Sample Size771
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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