A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2241n100



Internal ID22788328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20327352..20411461hg38UCSC Ensembl
chr15:20532605..20616714hg19UCSC Ensembl
chr15:18792619..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3884110
hg1984110
hg1884110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046913, nsv1037518, nsv1042220, nsv1048392
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2241n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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