A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054383



Internal ID18796914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44874619hg38UCSC Ensembl
Innerchr10:45210690..45370067hg19UCSC Ensembl
Innerchr10:44530696..44690073hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38159378
hg19159378
hg18159378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv729n100
Supporting Variantsnssv3707804
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)nsv1054383
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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