A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528055



Internal ID15455348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37594220..37595728hg38UCSC Ensembl
Innerchr21:38966522..38968030hg19UCSC Ensembl
Innerchr21:37888392..37889900hg18UCSC Ensembl
Innerchr21:37888392..37889900hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg381509
hg191509
hg181509
hg171509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704589
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528055
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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