A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053903



Internal ID18796434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50024819..50404231hg38UCSC Ensembl
Innerchr10:51784579..52163991hg19UCSC Ensembl
Innerchr10:51454585..51833997hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38379413
hg19379413
hg18379413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv853n100
Supporting Variantsnssv3520348
Samples
Known GenesASAH2, FAM21A, FAM21B, FLJ31813, SGMS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053903
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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