A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4311n100



Internal ID22790398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42542436..42674565hg38UCSC Ensembl
chr20:41171076..41303205hg19UCSC Ensembl
chr20:40604490..40736619hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38132130
hg19132130
hg18132130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063974, nsv1063513
Samples
Known GenesPTPRT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4311n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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