A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048652



Internal ID18791183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46289800hg38UCSC Ensembl
Innerchr10:47541177..47661036hg19UCSC Ensembl
Innerchr10:47011183..47131042hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38119860
hg19119860
hg18119860
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3706015, nssv3522435, nssv3508154
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)nsv1048652
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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