A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044108



Internal ID18786639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46306562hg38UCSC Ensembl
Innerchr10:47541177..47677798hg19UCSC Ensembl
Innerchr10:47011183..47147804hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38136622
hg19136622
hg18136622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv833n100
Supporting Variantsnssv3516222, nssv3506713, nssv3508113
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)nsv1044108
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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