A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551185



Internal ID16338594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63521170..63521755hg38UCSC Ensembl
Innerchr10:65280930..65281515hg19UCSC Ensembl
Innerchr10:64950936..64951521hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38586
hg19586
hg18586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1202n54
Supporting Variantsnssv748928
Samples
Known GenesREEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551185
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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