A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483034



Internal ID15582147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18917213..19081836hg38UCSC Ensembl
Innerchr21:20289531..20454154hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38164624
hg19164624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996225
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483034
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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