A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552159



Internal ID16339568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106773600..106871351hg38UCSC Ensembl
Innerchr10:108533358..108631109hg19UCSC Ensembl
Innerchr10:108523348..108621099hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3897752
hg1997752
hg1897752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv758413
Samples
Known GenesSORCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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