A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014245



Internal ID19103466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24784413..24843520hg38UCSC Ensembl
Innerchr1:25110904..25170011hg19UCSC Ensembl
Innerchr1:24983491..25042598hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3859108
hg1959108
hg1859108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3476665
Samples
Known GenesCLIC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014245
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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