A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552108



Internal ID16339517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106191058..106191792hg38UCSC Ensembl
Innerchr10:107950816..107951550hg19UCSC Ensembl
Innerchr10:107940806..107941540hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38735
hg19735
hg18735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1380n54
Supporting Variantsnssv757712, nssv757711
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552108
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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