A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046532



Internal ID19135751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119942262..119993640hg38UCSC Ensembl
Innerchr10:121701774..121753152hg19UCSC Ensembl
Innerchr10:121691764..121743142hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3851379
hg1951379
hg1851379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513051
Samples
Known GenesMIR4682, SEC23IP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046532
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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