A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975792



Internal ID18264313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5956385..5966542hg38UCSC Ensembl
Innerchr10:5998348..6008505hg19UCSC Ensembl
Innerchr10:6038354..6048511hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810158
hg1910158
hg1810158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759329
SamplesHGDP00998
Known GenesIL15RA
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975792
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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