A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2347n100



Internal ID19012715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20868184..22095238hg38UCSC Ensembl
chr15:21073513..22383189hg19UCSC Ensembl
chr15:19338171..19884553hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381227055
hg191309677
hg18546383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038878, nsv1050913, nsv1041600, nsv1045393, nsv1048242, nsv1035318, nsv1040743, nsv1038054, nsv1050173, nsv1035417, nsv1044204, nsv1048271, nsv1038828, nsv1045707, nsv1045125, nsv1054420, nsv1040146
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N4, 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)dgv2347n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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