A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001668



Internal ID18744199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13278..66815hg38UCSC Ensembl
Innerchr4:13278..66707hg19UCSC Ensembl
Innerchr4:3278..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3853538
hg1953430
hg1853430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5056n100
Supporting Variantsnssv3615229, nssv3615230, nssv3738056, nssv3738053, nssv3738055, nssv3738054
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)nsv1001668
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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