A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050724



Internal ID18793255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46175087..46281567hg38UCSC Ensembl
Innerchr10:47546323..47652803hg19UCSC Ensembl
Innerchr10:47016329..47122809hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38106481
hg19106481
hg18106481
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3514632, nssv3507937, nssv3706064
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050724
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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