A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514119



Internal ID18465714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44878497hg38UCSC Ensembl
Innerchr10:45210690..45373945hg19UCSC Ensembl
Innerchr10:44530696..44693951hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38163256
hg19163256
hg18163256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044334
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)nssv3514119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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