A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552104



Internal ID16339513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106190953..106191690hg38UCSC Ensembl
Innerchr10:107950711..107951448hg19UCSC Ensembl
Innerchr10:107940701..107941438hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38738
hg19738
hg18738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1380n54
Supporting Variantsnssv756254
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552104
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer