A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522265



Internal ID6024955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15494177..15546213hg19UCSC Ensembl
Innerchr6:15602156..15654192hg18UCSC Ensembl
Innerchr6:15602156..15654192hg17UCSC Ensembl
Cytoband6p22.3
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 Variantsnssv695045
Samples
Known GenesDTNBP1, JARID2
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)nsv522265
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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