A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050983



Internal ID18793514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5921958..6010233hg38UCSC Ensembl
Innerchr10:5963921..6052196hg19UCSC Ensembl
Innerchr10:6003927..6092202hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3888276
hg1988276
hg1888276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv666n100
Supporting Variantsnssv3497539
Samples
Known GenesFBXO18, IL15RA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050983
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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