A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012907



Internal ID19102124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65726020..65763257hg38UCSC Ensembl
Innerchr4:66591738..66628975hg19UCSC Ensembl
Innerchr4:66274333..66311570hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3837238
hg1937238
hg1837238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5238n100
Supporting Variantsnssv3740179, nssv3626014
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012907
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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