A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2173n100



Internal ID22788260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19811063..20373156hg38UCSC Ensembl
chr15:20016316..20578409hg19UCSC Ensembl
chr15:18276329..18838423hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38562094
hg19562094
hg18562095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041926, nsv1054484, nsv1044690
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2173n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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