A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004352



Internal ID18746883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65773..113230hg38UCSC Ensembl
Innerchr4:65665..113115hg19UCSC Ensembl
Innerchr4:55665..103115hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3847458
hg1947451
hg1847451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5069n100
Supporting Variantsnssv3615283
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004352
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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