A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522592



Internal ID6025797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43574936..43615505hg19UCSC Ensembl
Innerchr10:42894942..42935511hg18UCSC Ensembl
Innerchr10:42894942..42935511hg17UCSC Ensembl
Cytoband10q11.21
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 Variantsnssv705982
Samples
Known GenesRET
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)nsv522592
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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