A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053322



Internal ID18795853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4237109..4264606hg38UCSC Ensembl
Innerchr10:4279301..4306798hg19UCSC Ensembl
Innerchr10:4269301..4296798hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3827498
hg1927498
hg1827498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv662n100
Supporting Variantsnssv3493146, nssv3483382
Samples
Known GenesLINC00702
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053322
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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