A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509980



Internal ID18461575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46203032..46332377hg38UCSC Ensembl
Innerchr10:47574268..47703613hg19UCSC Ensembl
Innerchr10:47044274..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38129346
hg19129346
hg18129346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043463
Supporting Variants
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)nssv3509980
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