A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552158



Internal ID16339567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106727422..107842134hg38UCSC Ensembl
Innerchr10:108487180..109601892hg19UCSC Ensembl
Innerchr10:108477170..109591882hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381114713
hg191114713
hg181114713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1391n54
Supporting Variantsnssv758412
Samples
Known GenesSORCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552158
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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