A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054569



Internal ID18797100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132009350..132351508hg38UCSC Ensembl
Innerchr10:133822854..134165012hg19UCSC Ensembl
Innerchr10:133672844..134015002hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38342159
hg19342159
hg18342159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706259
Samples
Known GenesDPYSL4, JAKMIP3, LRRC27, STK32C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054569
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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