A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049800



Internal ID19139019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24083828..24102180hg38UCSC Ensembl
Innerchr10:24372757..24391109hg19UCSC Ensembl
Innerchr10:24412763..24431115hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818353
hg1918353
hg1818353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv690n100
Supporting Variantsnssv3707718, nssv3707719, nssv3511583, nssv3520143
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049800
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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