A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522773



Internal ID6025630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161152449..161170835hg19UCSC Ensembl
Innerchr6:161072439..161090825hg18UCSC Ensembl
Innerchr6:161122860..161141246hg17UCSC Ensembl
Cytoband6q26
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 Variantsnssv698414
Samples
Known GenesPLG
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)nsv522773
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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