A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2295n100



Internal ID19012663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20614753..20844186hg38UCSC Ensembl
chr15:20820055..21049515hg19UCSC Ensembl
chr15:19080069..19314115hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38229434
hg19229461
hg18234047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036455, nsv1041780, nsv1040125, nsv1035317, nsv1041283, nsv1038984, nsv1047725
Samples
Known GenesCXADRP2, LOC646214, NBEAP1, 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)dgv2295n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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