A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493146



Internal ID18734101
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 StatusS
Merged Variantsnsv1053322
Supporting Variants
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)nssv3493146
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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