A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052697



Internal ID19141916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38407736..38737005hg38UCSC Ensembl
Innerchr10:38696664..39030136hg19UCSC Ensembl
Innerchr10:38736670..39070142hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38329270
hg19333473
hg18333473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv709n100
Supporting Variantsnssv3515140
Samples
Known GenesACTR3BP5, LINC00999
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052697
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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