A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065411



Internal ID19154630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42552439..42606274hg38UCSC Ensembl
Innerchr20:41181079..41234914hg19UCSC Ensembl
Innerchr20:40614493..40668328hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3853836
hg1953836
hg1853836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4310n100
Supporting Variantsnssv3584798
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)nsv1065411
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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