A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014389



Internal ID18756923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..121670hg38UCSC Ensembl
Innerchr4:68809..121550hg19UCSC Ensembl
Innerchr4:58809..111550hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3852754
hg1952742
hg1852742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5069n100
Supporting Variantsnssv3616063, nssv3616049, nssv3616051, nssv3616050, nssv3616054, nssv3738082, nssv3616060, nssv3616056, nssv3738081, nssv3616055, nssv3616062, nssv3738089, nssv3738084, nssv3616045, nssv3616041, nssv3616040, nssv3616061, nssv3616047, nssv3616053, nssv3616048, nssv3616043, nssv3616057, nssv3616046, nssv3738088, nssv3616058, nssv3738083, nssv3738087, nssv3738085, nssv3738090, nssv3616042, nssv3616052, nssv3738086, nssv3738080, nssv3616059, nssv3616044
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)nsv1014389
Frequency
Sample Size29084
Observed Gain35
Observed Loss0
Observed Complex0
Frequencyn/a


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