A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041261



Internal ID18783792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5920672..6010233hg38UCSC Ensembl
Innerchr10:5962635..6052196hg19UCSC Ensembl
Innerchr10:6002641..6092202hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3889562
hg1989562
hg1889562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv666n100
Supporting Variantsnssv3499404
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)nsv1041261
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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