A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584799



Internal ID18883080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42556498..42664148hg38UCSC Ensembl
Innerchr20:41185138..41292788hg19UCSC Ensembl
Innerchr20:40618552..40726202hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38107651
hg19107651
hg18107651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063974
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)nssv3584799
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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