A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519436



Internal ID15446729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5955857..5966650hg38UCSC Ensembl
Innerchr10:5997820..6008613hg19UCSC Ensembl
Innerchr10:6037826..6048619hg18UCSC Ensembl
Innerchr10:6037826..6048619hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810794
hg1910794
hg1810794
hg1710794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705266, nssv695508, nssv692418, nssv673982, nssv656196, nssv697046
Samples
Known GenesIL15RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519436
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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