A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526774



Internal ID6025219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:27454995..27462727hg19UCSC Ensembl
Innerchr21:26376866..26384598hg18UCSC Ensembl
Innerchr21:26376866..26384598hg17UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv703126
Samples
Known GenesAPP
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv526774
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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