A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034718



Internal ID19123939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161031076..161108645hg38UCSC Ensembl
Innerchr4:161952228..162029797hg19UCSC Ensembl
Innerchr4:162171678..162249247hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3877570
hg1977570
hg1877570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5456n100
Supporting Variantsnssv3634139
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)nsv1034718
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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