A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2331n100



Internal ID19012699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20802132..21997806hg38UCSC Ensembl
chr15:21007461..22285757hg19UCSC Ensembl
chr15:19267484..19787121hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381195675
hg191278297
hg18519638
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036466, nsv1044568
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2331n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss5
Observed Complex0
Frequencyn/a


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