A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747341



Internal ID15694611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44873696hg38UCSC Ensembl
Innerchr10:45210690..45369144hg19UCSC Ensembl
Innerchr10:44530696..44689150hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38158455
hg19158455
hg18158455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550708
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747341
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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