A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041093



Internal ID18783624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118689033..119198373hg38UCSC Ensembl
Innerchr10:120448545..120957885hg19UCSC Ensembl
Innerchr10:120438535..120947875hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38509341
hg19509341
hg18509341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510865
Samples
Known GenesCACUL1, EIF3A, FAM45A, FAM45B, NANOS1, PRDX3, SFXN4, SNORA19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041093
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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