A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063422



Internal ID19152641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42466897..42485700hg38UCSC Ensembl
Innerchr20:41095537..41114340hg19UCSC Ensembl
Innerchr20:40528951..40547754hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3818804
hg1918804
hg1818804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584784
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)nsv1063422
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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