A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061399



Internal ID19150618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55458624..55497034hg38UCSC Ensembl
Innerchr20:54075162..54113572hg19UCSC Ensembl
Innerchr20:53508569..53546979hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3838411
hg1938411
hg1838411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584232
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)nsv1061399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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