A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063589



Internal ID19152808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:22077666..22241687hg38UCSC Ensembl
Innerchr21:23449985..23614007hg19UCSC Ensembl
Innerchr21:22371856..22535878hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38164022
hg19164023
hg18164023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599887
Samples
Known GenesLINC00308
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063589
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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