A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv247n21



Internal ID22766439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42555369..42669053hg38UCSC Ensembl
chr20:41184009..41297693hg19UCSC Ensembl
chr20:40617423..40731107hg18UCSC Ensembl
chr20:40617423..40731107hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38113685
hg19113685
hg18113685
hg17113685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526415, nsv528161
Samples
Known GenesPTPRT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv247n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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