A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525927



Internal ID15106534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6017935..6036116hg38UCSC Ensembl
Innerchr10:6059898..6078079hg19UCSC Ensembl
Innerchr10:6099904..6118085hg18UCSC Ensembl
Innerchr10:6099904..6118085hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3818182
hg1918182
hg1818182
hg1718182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702131
Samples
Known GenesIL2RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525927
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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