A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059573



Internal ID19148792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55096522..55301790hg38UCSC Ensembl
Innerchr20:53713061..53918329hg19UCSC Ensembl
Innerchr20:53146468..53351736hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38205269
hg19205269
hg18205269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584222
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059573
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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