A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483056



Internal ID15582169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20688190..20859445hg38UCSC Ensembl
Innerchr21:22060504..22231763hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38171256
hg19171260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996198
Samples
Known GenesLINC00320
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483056
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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