A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010357



Internal ID19099574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65726020..65773570hg38UCSC Ensembl
Innerchr4:66591738..66639288hg19UCSC Ensembl
Innerchr4:66274333..66321883hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3847551
hg1947551
hg1847551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5238n100
Supporting Variantsnssv3626037
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)nsv1010357
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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