A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060659



Internal ID19149878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18998152..19032598hg38UCSC Ensembl
Innerchr21:20370470..20404917hg19UCSC Ensembl
Innerchr21:19292341..19326788hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3834447
hg1934448
hg1834448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4394n100
Supporting Variantsnssv3599815
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)nsv1060659
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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