A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051687



Internal ID19140906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65566296..65584185hg38UCSC Ensembl
Innerchr10:67326054..67343943hg19UCSC Ensembl
Innerchr10:66996060..67013949hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3817890
hg1917890
hg1817890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv891n100
Supporting Variantsnssv3512749, nssv3522670
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051687
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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