A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705639



Internal ID15095605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46566170..46630476hg38UCSC Ensembl
Innerchr21:47986083..48050388hg19UCSC Ensembl
Innerchr21:46810511..46874816hg18UCSC Ensembl
Innerchr21:46810511..46874816hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3864307
hg1964306
hg1864306
hg1764306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528947
Supporting Variants
Samples
Known GenesDIP2A, S100B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705639
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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