A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549907



Internal ID16337316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5958296..5960405hg38UCSC Ensembl
Innerchr10:6000259..6002368hg19UCSC Ensembl
Innerchr10:6040265..6042374hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382110
hg192110
hg182110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743525
Samples
Known GenesIL15RA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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