A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052669



Internal ID18795200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44712577..44878497hg38UCSC Ensembl
Innerchr10:45208025..45373945hg19UCSC Ensembl
Innerchr10:44528031..44693951hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38165921
hg19165921
hg18165921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv729n100
Supporting Variantsnssv3517452, nssv3503482
Samples
Known GenesTMEM72-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052669
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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