A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053934



Internal ID18796465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101409846..101691479hg38UCSC Ensembl
Innerchr10:103169603..103451236hg19UCSC Ensembl
Innerchr10:103159593..103441226hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38281634
hg19281634
hg18281634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521114
Samples
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053934
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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