A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046108



Internal ID18788639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46291524hg38UCSC Ensembl
Innerchr10:47541177..47662760hg19UCSC Ensembl
Innerchr10:47011183..47132766hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38121584
hg19121584
hg18121584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv833n100
Supporting Variantsnssv3504842, nssv3509709
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046108
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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