A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550491



Internal ID16337900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38577087..38729937hg38UCSC Ensembl
Innerchr10:38870218..39023068hg19UCSC Ensembl
Innerchr10:38910224..39063074hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38152851
hg19152851
hg18152851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1053n54
Supporting Variantsnssv746975
Samples
Known GenesACTR3BP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550491
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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