A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584792



Internal ID18883073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42550060..42614384hg38UCSC Ensembl
Innerchr20:41178700..41243024hg19UCSC Ensembl
Innerchr20:40612114..40676438hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3864325
hg1964325
hg1864325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061179
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)nssv3584792
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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