A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007239



Internal ID19096458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16688..45414hg38UCSC Ensembl
Innerchr4:16688..45410hg19UCSC Ensembl
Innerchr4:6688..35410hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3828727
hg1928723
hg1828723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5051n100
Supporting Variantsnssv3738058
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)nsv1007239
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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