A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046088



Internal ID18788619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16786830..16906310hg38UCSC Ensembl
Innerchr10:16828829..16948309hg19UCSC Ensembl
Innerchr10:16868835..16988315hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38119481
hg19119481
hg18119481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517749
Samples
Known GenesCUBN, RSU1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046088
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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