A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522791



Internal ID15103398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41856674..41862327hg38UCSC Ensembl
Innerchr21:43276783..43282436hg19UCSC Ensembl
Innerchr21:42149852..42155505hg18UCSC Ensembl
Innerchr21:42149852..42155505hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385654
hg195654
hg185654
hg175654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698435
Samples
Known GenesPRDM15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522791
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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