A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022143



Internal ID19111361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184267146..184307462hg38UCSC Ensembl
Innerchr4:185188299..185228615hg19UCSC Ensembl
Innerchr4:185425293..185465609hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3840317
hg1940317
hg1840317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5492n100
Supporting Variantsnssv3635611
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)nsv1022143
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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