A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049834



Internal ID18792365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68410888..68752800hg38UCSC Ensembl
Innerchr10:70170645..70512557hg19UCSC Ensembl
Innerchr10:69840651..70182563hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38341913
hg19341913
hg18341913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv919n100
Supporting Variantsnssv3512292
Samples
Known GenesCCAR1, DNA2, SLC25A16, TET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049834
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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