A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051508



Internal ID19140727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131601825..131844996hg38UCSC Ensembl
Innerchr10:133434161..133677331hg19UCSC Ensembl
Innerchr10:133284151..133527321hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38243172
hg19243171
hg18243171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv991n100
Supporting Variantsnssv3520446
Samples
Known GenesFLJ46300
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051508
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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