A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483099



Internal ID15235573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43312087..43525657hg38UCSC Ensembl
Innerchr21:44731967..44945537hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38213571
hg19213571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996508
Samples
Known GenesLINC00313, LINC00319, LINC00322, SIK1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483099
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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