A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550788



Internal ID15991511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46234821..46332710hg38UCSC Ensembl
Innerchr10:47606057..47703946hg19UCSC Ensembl
Innerchr10:47076063..47173952hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3897890
hg1997890
hg1897890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1115n54
Supporting Variantsnssv747630
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550788
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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