A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552241



Internal ID16339650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121677182..121699130hg38UCSC Ensembl
Innerchr10:123436696..123458644hg19UCSC Ensembl
Innerchr10:123426686..123448634hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3821949
hg1921949
hg1821949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1406n54
Supporting Variantsnssv760308
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552241
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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