A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522199



Internal ID15449492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35668350..35728742hg38UCSC Ensembl
Innerchr21:37040648..37101040hg19UCSC Ensembl
Innerchr21:35962518..36022910hg18UCSC Ensembl
Innerchr21:35962518..36022910hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3860393
hg1960393
hg1860393
hg1760393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694972
Samples
Known GenesMIR802
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522199
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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