A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065892



Internal ID19155111
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 StatusM
Merged Variantsdgv4310n100
Supporting Variantsnssv3584789
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)nsv1065892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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