A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001623



Internal ID19090840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65726020..65770325hg38UCSC Ensembl
Innerchr4:66591738..66636043hg19UCSC Ensembl
Innerchr4:66274333..66318638hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3844306
hg1944306
hg1844306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5238n100
Supporting Variantsnssv3626036, nssv3626034, nssv3626035, nssv3740191, nssv3740189, nssv3740190
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)nsv1001623
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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