A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503482



Internal ID18455077
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 StatusS
Merged Variantsnsv1052669
Supporting Variants
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)nssv3503482
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