A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549909



Internal ID16337318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5976285..5978138hg38UCSC Ensembl
Innerchr10:6018248..6020101hg19UCSC Ensembl
Innerchr10:6058254..6060107hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381854
hg191854
hg181854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743527
Samples
Known GenesIL15RA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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