A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2170n100



Internal ID22788257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19811063..19958406hg38UCSC Ensembl
chr15:20016316..20163659hg19UCSC Ensembl
chr15:18276329..18423673hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38147344
hg19147344
hg18147345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036508, nsv1037097, nsv1048203, nsv1041096, nsv1049197, nsv1042589, nsv1037931
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2170n100
Frequency
Sample Size11257
Observed Gain52
Observed Loss0
Observed Complex0
Frequencyn/a


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