A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523466



Internal ID6026049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103547135..103567525hg19UCSC Ensembl
Innerchr7:103334371..103354761hg18UCSC Ensembl
Innerchr7:103141086..103161476hg17UCSC Ensembl
Cytoband7q22.1
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 Variantsnssv699225
Samples
Known GenesRELN
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)nsv523466
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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