A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584789



Internal ID18883070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42540046..42602092hg38UCSC Ensembl
Innerchr20:41168686..41230732hg19UCSC Ensembl
Innerchr20:40602100..40664146hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3862047
hg1962047
hg1862047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065892
Supporting Variants
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)nssv3584789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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