A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656196



Internal ID15046162
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519436
Supporting Variants
Samples
Known GenesIL15RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656196
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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