A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522320



Internal ID6023586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1857112..2018168hg19UCSC Ensembl
Innerchr11:1813688..1974744hg18UCSC Ensembl
Innerchr11:1813688..1974744hg17UCSC Ensembl
Cytoband11p15.5
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 Variantsnssv695100
Samples
Known GenesH19, LSP1, MIR4298, MIR675, MRPL23, MRPL23-AS1, SYT8, TNNI2, TNNT3
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)nsv522320
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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