A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551233



Internal ID16338642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65025888..65372541hg38UCSC Ensembl
Innerchr10:66785646..67132299hg19UCSC Ensembl
Innerchr10:66455652..66802305hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38346654
hg19346654
hg18346654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1212n54
Supporting Variantsnssv1174991
SamplesHGDP00145
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551233
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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