A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552092



Internal ID16339501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105333072..105562272hg38UCSC Ensembl
Innerchr10:107092830..107322030hg19UCSC Ensembl
Innerchr10:107082820..107312020hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38229201
hg19229201
hg18229201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1377n54
Supporting Variantsnssv756241
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552092
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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