A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006760



Internal ID19095978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65726020..65764255hg38UCSC Ensembl
Innerchr4:66591738..66629973hg19UCSC Ensembl
Innerchr4:66274333..66312568hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3838236
hg1938236
hg1838236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5238n100
Supporting Variantsnssv3740185, nssv3740181, nssv3740186, nssv3626021, nssv3626024, nssv3626025, nssv3740184, nssv3740182, nssv3740183, nssv3740187, nssv3626022, nssv3626023, nssv3626026
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)nsv1006760
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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